1 P5Y

Exhibit 99.1

 

YD BIO LIMITED

INDEX TO UNAUDITED INTERIM CONSOLIDATED FINANCIAL STATEMENTS

 

    Pages
Unaudited Consolidated Balance Sheets as of June 30, 2026 and December 31, 2025   1
Unaudited Consolidated Statements of Operations and Comprehensive Income/(Loss) for the Six Months Ended June 30, 2026 and 2025   2
Unaudited Consolidated Statements of Changes in Shareholders’ Equity (Deficits) for the Six Months Ended June 30, 2026 and 2025   3
Unaudited Consolidated Statements of Cash Flows for the Six Months Ended June 30, 2026 and 2025   4
Notes to Unaudited Consolidated Financial Statements   5

 

i

 

 

YD BIO LIMITED

UNAUDITED CONSOLIDATED BALANCE SHEETS

 

    Notes     As of
June 30,
2026
    As of
December 31,
2025
 
          US$     US$  
ASSETS                  
CURRENT ASSETS                  
Cash and cash equivalents             2,662,004       6,007,615  
Accounts receivable, net     4       223,067       167,477  
Due from affiliates     20       33,636       291,540  
Inventories     5       1,892,355       1,879,542  
Prepaid expenses and other current assets     6       780,309       1,324,016  
TOTAL CURRENT ASSETS             5,591,371       9,670,190  
                         
Operating lease right-of-use assets, net     10       6,681       8,470  
Property, plant and equipment, net     7       50,648       59,340  
Intangible assets     8       2,473,692       2,609,739  
Prepaid expenses, non-current     9       1,937,869       1,431,658  
TOTAL ASSETS             10,060,261       13,779,397  
                         
LIABILITIES                        
CURRENT LIABILITIES                        
Due to affiliates     20       358,864       785,665  
Operating lease liabilities, current     10       5,002       6,764  
Accounts payable     11       371,594       413,290  
Accrued expenses and other liabilities     12       333,411       437,859  
TOTAL CURRENT LIABILITIES             1,068,871       1,643,578  
                         
Warrant Liabilities     13,15       4,517,421       14,991,482  
TOTAL LIABILITIES             5,586,292       16,635,060  
                         
Commitments and contingencies     19                  
                         
SHAREHOLDERS’ EQUITY (DEFICIT)                        
Common shares ($0.0001 par value, 500,000,000 shares authorized; 70,842,844 and 70,789,261 issued and outstanding as of June 30, 2026 and December 31, 2025, respectively)     14       7,084       7,079  
Additional paid-in capital     14       7,862,430       7,161,681  
Accumulated deficits             (3,537,862 )     (10,238,359 )
Accumulated other comprehensive income             142,317       213,936  
Total shareholders’ equity (deficit)             4,473,969       (2,855,663 )
TOTAL LIABILITIES AND SHAREHOLDERS’ EQUITY (DEFICIT)             10,060,261       13,779,397  

  

The accompanying notes are an integral part of these unaudited consolidated financial statements. 

 

1

 

YD BIO LIMITED

 UNAUDITED CONSOLIDATED STATEMENTS OF OPERATIONS

 AND COMPREHENSIVE INCOME/(LOSS)

 

          For the Six Months Ended
June 30,
 
    Notes     2026     2025  
          US$     US$  
Revenue     16       846,501       204,007  
Cost of revenue             (578,271 )     (135,212 )
Gross profit             268,230       68,795  
                         
Operating expenses                        
General and administrative expenses             1,866,420       1,170,489  
Selling and marketing expenses             518,147       56,574  
Research and development expenses     8,17       1,113,766       791,456  
Impairment of expected credit loss     4       4,553       4,108  
Total operating expenses             3,502,886       2,022,627  
                         
Loss from operations             (3,234,656 )     (1,953,832 )
                         
Other income                        
Other income, net             35,916       17,305  
Interest income             52,705       18,439  
Change in fair value of warrant liabilities     15       9,846,532       -  
Total other income, net             9,935,153       35,744  
                         
Income (Loss) before income tax             6,700,497       (1,918,088 )
Income tax benefit     18       -       1,507  
Net income(loss)             6,700,497       (1,916,581 )
                         
Other comprehensive income (loss), net of tax:                        
Change in foreign currency translation adjustments             (71,619 )     414,486  
Other Comprehensive income (loss)             6,628,878       (1,502,095 )
                         
Basic and diluted net income (loss) per share             0.09       (0.03 )
Basic and diluted weighted average number of shares outstanding             70,827,822       64,730,411  

 

The accompanying notes are an integral part of these unaudited consolidated financial statements.

 

2

 

YD BIO LIMITED

UNAUDITED CONSOLIDATED STATEMENTS OF CHANGES IN SHAREHOLDERS’ EQUITY (DEFICITS)

For the six months ended June 30, 2026 and 2025

 

    Shares*     Amount     Additional
paid-in
capital
    Accumulated
deficits
    Accumulative
other
comprehensive
income
   

Total
Equity

(deficit)

 
          US$     US$     US$     US$     US$  
Balance at December 31, 2025     70,789,261       7,079       7,161,681       (10,238,359 )     213,936       (2,855,663 )
Issuance of Common Shares per Warrants exercise     37,923       3       640,751       —       —       640,754  
Issuance of Ordinary shares upon RSU settlement *     15,660       2       59,998       —       —       60,000  
Net income     —       —       —       6,700,497       —       6,700,497  
Foreign currency translation adjustment     —       —       —       —       (71,619 )     (71,619 )
Balance at June 30, 2026     70,842,844       7,084       7,862,430       (3,537,862 )     142,317       4,473,969  

 

* Includes 11,498 shares vested on June 30, 2026 administratively issued on July 1, 2026.

 

    Shares     Amount     Additional
paid-in
capital
    Accumulated
deficits
    Accumulative
other
comprehensive
income
    Total
Equity
 
          US$     US$     US$     US$     US$  
Balance at December 31, 2024     1,441,766       144,177       8,328,040       (1,927,043 )     45,072       6,590,246  
Recapitalization     63,288,645       (137,704 )     137,704       —       —       —  
Balance at December 31, 2024     64,730,411       6,473       8,465,744       (1,927,043 )     45,072       6,590,246  
Net loss     —       —       —       (1,916,581 )     —       (1,916,581 )
Foreign currency translation adjustment     —       —       —       —       414,486       414,486  
Balance at June 30, 2025     64,730,411       6,473       8,465,744       (3,843,624 )     459,558       5,088,151  

 

The accompanying notes are an integral part of these unaudited consolidated financial statements.

 

3

 

YD BIO LIMITED

UNAUDITED CONSOLIDATED STATEMENTS OF CASH FLOWS

 

          For the Six Months Ended
June 30,
 
    Notes     2026     2025  
          US$     US$  
CASH FLOWS FROM OPERATING ACTIVITIES:                  
Net Income (loss)             6,700,497       (1,916,581 )
Adjustments to reconcile net income (loss) to net cash used in operating activities                        
Deferred tax liability             —       (1,510 )
Depreciation expenses     7       8,477       8,043  
Amortization     8       95,748       95,142  
Impairment of expected credit loss     4       4,553       4,108  
Loss on disposal of property and equipment             3,927       —  
Lease expenses     10       10,139       19,187  
Stock based compensation             60,000       —  
Change in fair value of warrant liabilities     15       (9,846,532 )     —  
Changes in operating assets and liabilities                        
Accounts receivable             (60,143 )     (9,928 )
Inventories             (12,813 )     (332,878 )
Prepaid expense and other current assets             539,682       (157,138 )
Due from affiliates             257,904       (45,316 )
Accounts payable             (41,696 )     9,308  
Accrued expense and other liabilities             (104,448 )     150,684  
Amounts due to affiliates             (426,801 )     23,621  
Operating lease liabilities             (10,112 )     (8,620 )
Net cash used in operating activities             (2,821,618 )     (2,161,878 )
CASH FLOWS FROM INVESTING ACTIVITIES                        
Prepayments for real estate     9       (506,211 )     —  
Acquisition of property, plant and equipment     7       (8,069 )     (2,659 )
Net cash used in investing activities             (514,280 )     (2,659 )
                         
CASH FLOWS FROM FINANCING ACTIVITIES:                        
Proceeds from exercise of warrants             17,250       —  
Payment of offering cost related to business combination             —       (561,207 )
Net cash provided by (used in) financing activities             17,250       (561,207 )
                         
Effect of change in exchange rate             (26,963 )     62,966  
                         
NET DECREASE IN CASH AND CASH EQUIVALENTS             (3,345,611 )     (2,662,778 )
Cash and cash equivalents, beginning of period             6,007,615       3,132,298  
Cash and cash equivalents, end of period             2,662,004       469,520  
                         
SUPPLEMENTAL CASH FLOW INFORMATION                        
Income taxes paid             —       —  
Interest paid             —       —  

 

The accompanying notes are an integral part of these unaudited consolidated financial statements.

 

4

 

YD BIO LIMITED

NOTES TO UNAUDITED FINANCIAL STATEMENTS

 

1. ORGANIZATION

 

YD Bio Limited ("YD Bio" or the "Company") is as a Cayman Islands company operating under the Cayman Islands Companies Act (Revised) with its shares listed on NASDAQ ("symbol": YDES). YD Bio Limited is a publicly listed biotechnology company focused on regulated diagnostics, life science clinical services, and healthcare product commercialization. Its operations include oncology testing programs conducted through an affiliate laboratory and a telehealth platform, as well as distribution and regulatory liaison services for pharmaceutical clients. The Company also holds licensed limbal stem cell technologies and maintains healthcare commercialization operations in the U.S. and Asia.

 

Business Combination

 

On September 24, 2024, the Merger Agreement was signed among (i) the Company, (ii) Breeze Holdings Acquisition Corp., a Delaware corporation (“Breeze”), (iii) Breeze Merger Sub, Inc., a Delaware corporation and which will be a direct, wholly owned subsidiary of the Company (“Breeze Merger Sub”), (iv) BH Biopharma Merger Sub Limited, a Cayman Islands exempted company (“Company Merger Sub,” with Company Merger Sub and Breeze Merger Sub together referred to herein as the “Merger Subs”), and (v) YD Biopharma Limited, a Cayman Islands exempted company (“YD Biopharma”). In connection with and upon the consummation of the merger contemplated by the Merger Agreement, Breeze Merger Sub will merge with and into Breeze with Breeze surviving the merger as a wholly-owned subsidiary of the Company, and Company Merger Sub will merge with and into YD Biopharma, with YD Biopharma surviving such merger as a wholly-owned subsidiary of the Company. The Merger and the other transactions contemplated by the Merger Agreement are collectively referred to as the “Business Combination”.

 

On August 28, 2025 (the “Closing Date”), the Company consummated the closing of the Business Combination.

 

As a result of the Business Combination, the Company is the surviving publicly traded entity and owns 100% of the outstanding ordinary shares of YD Biopharma and ordinary shares, warrants, and rights of Breeze. Breeze’s outstanding shares were exchanged for 4,140,948 ordinary shares of the Company, as stipulated in the Merger Agreement. This exchange reflects the conversion of Breeze’s public shares, sponsor shares, rights and other outstanding equity interests (net of any redemptions) into ordinary shares of the Company, contributing to the post-closing equity structure of the Company.

 

At the same time, pursuant to the Merger Agreement, the issued and outstanding shares of YD Biopharma were exchanged for ordinary shares of the Company with each YD Biopharma shareholder receiving its pro rata share of the Exchange Consideration. The “Exchange Consideration” was the number of newly issued YD Bio ordinary shares equal to (a) a transaction value of $647,304,110 divided by (b) a per share price of $10.00. “Pro Rata Share” means, with respect to each YD Biopharma shareholder, a fraction expressed as a percentage equal to (i) the number of shares of common stock held by such YD Biopharma shareholder immediately prior to the closing, divided by (ii) the total number of issued and outstanding shares of common stock immediately prior to the closing. As a result, 64,730,411 ordinary shares of the Company were issued to the former shareholders of YD Biopharma at closing.

 

5

 

In addition, on August 28, 2025, the Company issued 1,650,000 ordinary shares to certain investors in connection with a private investment in public equity (“PIPE”) Financing raising aggregate proceeds of $13.2 million at a price per share of $8.00.

  

On August 28, 2025, Breeze’s outstanding warrants were exchanged for 16,925,000 YD Bio warrants on a one-for-one basis, with the same exercise price and terms.

 

As of August 28, 2025, immediately following the completion of the Business Combination closing, there were 70,521,359 ordinary shares outstanding and 16,925,000 warrants outstanding.

 

The transaction was accounted for as a reverse recapitalization with YD Biopharma being the accounting acquirer and Breeze as the acquired company for accounting purposes. YD Biopharma was determined to be the accounting acquirer since YD Biopharma’s shareholders prior to the Business Combination had the greatest voting interest in the combined entity, YD Biopharma comprised the ongoing operations, had the go-forward senior management, and the YD Biopharma shareholders were to control the board of directors and have a majority of the voting power of YD Bio. Accordingly, for accounting purposes, the financial statements after the closing of the Business Combination represent a continuation of the financial statements of YD Biopharma, with the Business Combination treated as the equivalent of issuing shares for the net assets of Breeze, accompanied by a recapitalization. The net assets of Breeze are stated at historical cost, with no goodwill or other intangible assets recorded. Additionally, the shares and corresponding capital amounts and losses per share, prior to the Business Combination have been retrospectively restated base on shares reflecting the exchange ratio established in Merger Agreement.

 

On August 29, 2025, the Ordinary Shares and Public Warrants began trading on the NASDAQ under the proposed symbols “YDES” and “YDESW,” respectively.

 

Breeze was liquidated in December 2025. As at the date of this report, the Company has direct and indirect interests in the following subsidiaries:

 

Name of Entity   Date of
Incorporation
  Place of
Incorporation
  Shareholders   % of
Equity
Ownership
  Principal
Activities
YD Biopharma Limited (“YD Biopharma”)   March 14, 2024   Cayman   YD Bio   100%   Holding
Yong Ding Biopharm Co., Ltd (“Yong Ding”)   April 23, 2013   the Republic of China (“ROC” or “Taiwan”)   YD Biopharma   100%   Sales of drugs, medical and related products in Taiwan
YD BIO USA, INC. (“YD BIO USA”)   February 4, 2025   Delaware (US)   YD Biopharma   100%   Sales of drugs, medical and related products in US
YD PharmaWings Limited (“YD PharmaWings”)   October 23, 2025   BVI   YD Biopharma   100%   Investment holding

 

2. GOING CONCERN

 

In connection with the Company’s assessment of going concern considerations in accordance with the authoritative guidance in Financial Accounting Standard Board (“FASB”) Accounting Standards Update (“ASU”) Topic 2014-15, “Disclosures of Uncertainties about an Entity’s Ability to Continue as a Going Concern,” management has determined that the Company currently lacks the liquidity it needs to sustain operations for a reasonable period of time, which is considered to be at least one year from the date that the consolidated financial statements are issued

 

The Company’s financial statements have been prepared on a going concern basis, which contemplates the realization of assets and liquidation of liabilities during the normal course of operations. The Company’s operating results for future periods are subject to numerous uncertainties and it is uncertain if the Company will be able to generate net income for the foreseeable future. Accordingly, the Company may not be able to obtain additional financing. These conditions raise substantial doubt about the Company’s ability to continue as a going concern for at least twelve months from the date of the interim financial statements were issued.

 

6

 

The Company has incurred recurring losses (excluding the fair value changes of warrant liabilities) and negative cash flows from operations for the six months ended June 30, 2026 and 2025. The Company will need additional funds to satisfy its outstanding payables, fund its working capital, and fully implement its business plan.

 

The Company plans to continue developing strategies on similar or expanded operations of business to help our ability to determine where business will be viable going forward. Until such time, if ever, the Company can generate substantial product revenues. The Company plans to finance cash needs through public or private equity offerings or debt financing.

 

However, there is no assurance that the Company will be able to raise additional capital, generate revenues or achieve profitability due to the factors listed above.

 

The accompanying unaudited consolidated financial statements do not include any adjustments to reflect the possible future effects on the recoverability and classification of assets or the amounts and classification of liabilities that may result from the outcome of these or other risks or uncertainties.

 

3. SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

 

Basis of Presentation

 

The accompanying unaudited consolidated financial statements have been prepared in accordance with generally accepted accounting principles in the United States of America (GAAP) for interim financial information. Accordingly, they do not include all the information and footnotes required by GAAP for the annual consolidated financial statements and should be read in conjunction with the annual consolidated financial statements of 20-F filed with SEC on April 30, 2026.

 

Preparation of these financial statements requires Management to make judgments, estimates and assumptions based on existing knowledge that affects the application of accounting policies and reported amounts and disclosures. Actual results could differ from these estimates and assumptions. Estimates and underlying assumptions are reviewed on an ongoing basis. Revisions to accounting estimates are recognized in the period in which the estimates are revised and in any future periods affected.

 

Emerging Growth Company Status

 

The Company is an emerging growth company, as defined in the Jumpstart Our Business Startups Act of 2012 (the “JOBS Act”). Under the JOBS Act, emerging growth companies can delay adopting new or revised accounting standards issued subsequent to the enactment of the JOBS Act until such time as those standards apply to private companies. The Company has elected to avail itself of this exemption and, therefore, for new or revised accounting standards applicable to public companies, the Company will be subject to an extended transition period until those standards would otherwise apply to private companies.

 

Business combination

 

The Company applies the provisions of ASC 805, Business Combinations, in accounting for its acquisitions. To determine whether transactions should be accounted for as asset acquisition or business combination, the Company evaluates whether substantially all of the fair value of gross assets included in a transaction is concentrated in a single asset (or a group of similar assets), resulting in an asset acquisition; if that is not the case, the resulting accounting is as a business combination. In an asset acquisition, the cost of acquiring the asset group, including transaction costs, is allocated to the acquired assets or assumed liabilities based on their relative fair values without giving rise to goodwill. In a business combination, the Company recognizes separately from goodwill the assets acquired and the liabilities assumed at their acquisition date fair values. Goodwill as of the acquisition date is measured as the excess of consideration transferred over the net of the acquisition date fair values of the assets acquired and the liabilities assumed. While the Company uses its best estimates and assumptions to accurately value assets acquired and liabilities assumed at the acquisition date as well as any contingent consideration, where applicable, its estimates are inherently uncertain and subject to refinement. As a result, during the measurement period, which may be up to one year from the acquisition date, the Company records adjustments to the assets acquired and liabilities assumed with the corresponding offset to goodwill. Upon the conclusion of the measurement period or final determination of the values of assets acquired or liabilities assumed, whichever comes first, any subsequent adjustments are recorded to its consolidated statements of operations.

 

7

 

The Business Combination was accounted for as a “reverse recapitalization” in accordance with accounting principles generally accepted in GAAP. Under this method of accounting, Breeze was treated as the “acquired” company for financial reporting purposes. YD Biopharma was determined to be the accounting acquirer since YD Biopharma’s shareholders prior to the Business Combination had the greatest voting interest in the combined entity, YD Biopharma comprised the ongoing operations, had the go-forward senior management, and the YD Biopharma shareholders were to control the board of directors and have a majority of the voting power of YD Bio. Accordingly, for accounting purposes, the financial statements after the closing of the Business Combination represent a continuation of the financial statements of YD Biopharma, with the Business Combination treated as the equivalent of issuing shares for the net assets of Breeze, accompanied by a recapitalization. The net assets of Breeze are stated at historical cost, with no goodwill or other intangible assets recorded.

 

Principles of consolidation  

 

The financial statements include the financial statements of the Company and its subsidiaries, see Note 1.

 

Use of estimates

 

The preparation of the unaudited consolidated financial statements in conformity with GAAP requires the Company’s management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting period.

 

Making estimates requires management to exercise significant judgment. It is at least reasonably possible that the estimate of the effect of a condition, situation or set of circumstances that existed at the date of the financial statements, which management considered in formulating its estimate, could change in the near term due to one or more future confirming events. Significant accounting estimates reflected in the unaudited consolidated financial statements included revenue recognition, provision for expected credit losses of accounts receivable, prepayment and other receivables, inventories impairment assessment, property, plant and equipment impairment assessment, intangible assets impairment assessment, the valuation allowance for deferred tax assets, right-of-use (“ROU”) assets and operating lease liabilities. Accordingly, the actual results could differ significantly from those estimates. 

 

Risk and uncertainties

 

Generally, the industry in which the Company operates subjects the Company to a number of risks and uncertainties that can affect its operating results and financial condition. Such factors include, but are not limited to: the timing, costs and results of clinical trials and other development activities versus expectations; the ability to manufacture products successfully; competition from products sold or being developed by other companies; the price of, and demand for products once approved; the ability to negotiate favorable licensing or other manufacturing and marketing agreements for its products.

 

Fair Value of Financial Instruments

 

The Company has adopted Financial Accounting Standards Board (“FASB”) Accounting Standards Codification (“ASC”) 820, Fair Value Measurements, which defines fair value, establishes a framework for measuring fair value in U.S. GAAP, and expands disclosures about fair value measurements. ASC 820 establishes a three-level valuation hierarchy of valuation techniques based on observable and unobservable input, which may be used to measure fair value and include the following:

 

  Level 1 — Quoted prices in active markets for identical assets or liabilities.

 

  Level 2 — Input other than Level 1 that is observable, either directly or indirectly, such as quoted prices for similar assets or liabilities; quoted prices in markets that are not active; or other input that is observable or can be corroborated by observable market data for substantially the full term of the assets or liabilities.

 

  Level 3 — Unobservable input that is supported by little or no market activity and that is significant to the fair value of the assets or liabilities.

 

8

  

The measurement of Warrants is classified as Level 1 due to the use of an observable market quote in an active market under the ticker YDESW.

 

The carrying amounts of the other financial assets and liabilities, which consist of accounts receivable, other current assets, accounts payable and other liabilities, amount due to a shareholder and amount due to an affiliate, approximate their fair values due to the short-term nature of these instruments.

 

Cash and cash equivalents

 

Cash and cash equivalents included cash on hand placed with banks or other financial institutions, which are unrestricted as to withdrawal and use and with an original maturity of three months or less. Cash equivalents are short-term, highly liquid investments that are readily convertible into cash with an original maturity of three months or less, at the date acquired.

 

Deposits in banks in Taiwan are only insured by Central Deposit Insurance Corporation, a government agency, up to NTD 3 million (US$94,000); Deposit in banks in the USA are only insured by Federal Deposit Insurance Corporation up to $250,000 and are consequently exposed to risk of loss. As of June 30, 2026 and December 31, 2025, the Company’s balance of cash and cash equivalents was comprised solely of cash in the amount of $2.6 million and $6.0 million, respectively, with no cash equivalents included.

 

Receivable and Allowance

 

The Company has adopted ASC 326, Financial Instruments — Credit Losses, which requires an impairment model that is based on current expected loss.

 

The Company’s accounts receivable and other current assets are within the scope of ASC 326. Accounts receivable and amount due from an affiliate are recognized and carried at the original invoice amounts less the expected credit loss. The Company has a policy of reserving for uncollectible accounts based on best estimate of the amount of probable expected credit losses in the existing accounts receivable. The Company performs ongoing credit evaluations of its customers and maintains an allowance for potential bad debts if required. Other current assets are recognized and carried at the initial amount when occurred less an allowance for any uncollectible amount. To estimate expected credit losses, the Company has identified the relevant risk characteristics of its counterparty and the related receivables, amount due from an affiliate and other current assets which include size, type of the services or the products the Company provides, or a combination of these characteristics. Receivables with similar risk characteristics have been grouped into pools. For each pool, the Company considers the past collection experience, current economic conditions, future economic conditions (external data and macroeconomic factors) and changes in the Company’s customer collection trends. Other key factors that influence the expected credit loss analysis include customer demographics, payment terms offered in the normal course of business to customers, and industry-specific factors that could impact the Company’s receivables. Additionally, external data and macroeconomic factors are also considered. This is assessed annually based on the Company’s specific facts and circumstances. There has been no significant impact of changes in the assumptions since adoption. The Company has assessed its receivable and amount due from an affiliate including credit term and corresponding receivables as of June 30, 2026. Based upon such credit terms, the Company recorded bad debt expenses of $4,553 and $4,108 for the six months ended June 30, 2026 and 2025, respectively. The Company recognized $11,019 and $6,598 expected credit loss provision for account receivables and other current assets as of June 30, 2026 and December 31, 2025, respectively.

  

Inventories

 

Inventories are stated at the lower of cost and net realizable value, with cost determined by the weighted average method. Net realizable value is the estimated selling prices in the ordinary course of business, less reasonably predictable costs of completion, disposal, and transportation. Write-down of potential obsolete or slow-moving inventories is recorded as cost of revenue based on management’s assumptions about future demands and market conditions. No write-down is recorded for inventories for the six months ended June 30, 2026 and 2025.

 

9

 

Property, Plant and Equipment

 

Property, plant and equipment are stated at cost less accumulated depreciation and impairment losses, if any. Depreciation is computed on a straight-line basis with no salvage value over the estimated useful lives of 3 to 5 years for equipment, fixtures and furniture.

 

The cost and accumulated depreciation of property, plant and equipment disposed of or sold are removed from the balance sheets and the resulting gains and losses are recognized in the statements of operations.

 

Intangible assets

 

Intangible assets are stated in the balance sheet at cost less accumulated amortization and impairment, if any. The costs of the intangible assets are amortized on straight-line basis over their estimated useful lives. The Company had two licensed patents as of June 30, 2026, (i) one licensed patent involves the formula and technology of cell culture process, technology of cell bank construction, exosome purification, authentication technology, and exosome production which are derived from the methods of culturing human corneal limbus cells and the relevant know-how (the “3D Global Patent”) and (ii) the other licensed patent involves Methylation analysis technology for application in pancreatic cancer and the relevant know-how (the “EG BioMed Patent”).

 

The respective amortization periods for the intangible assets are as follows:

 

3D Global Patent (note 8)   15 years
EG BioMed Patent (note 8)   15 years

 

Impairment of Long-Lived Assets

 

In accordance with the ASC 360-10, Accounting for the Impairment or Disposal of Long-Lived Assets, long-lived assets, such as property, plant and equipment, leased assets and purchased intangible assets subject to amortization are reviewed for impairment whenever events or changes in circumstances indicate that the carrying value of an asset may not be recoverable, or it is reasonably possible that these assets could become impaired as a result of technological or other industrial changes. The determination of recoverability of assets to be held and used is made by comparing the carrying amount of an asset to future undiscounted cash flows to be generated by the assets.

 

If such assets are considered to be impaired, the impairment to be recognized is measured as the amount by which the carrying amount of the assets exceeds the fair value of the assets. Assets uposed of are reported at the lower of the carrying amount or fair value less cost to sell. There was no impairment of long-lived assets recorded for the six months ended June 30, 2026 and 2025.

 

Lease

 

The Company accounts for leases in accordance with ASC 842, Leases, which requires lessees to recognize leases on the balance sheet and disclose key information about leasing arrangements. For the leases with a term within 12 months, the Company has elected the short-term lease recognition exemption and therefore does not recognize right-of-use (ROU) assets or lease liabilities for these leases.

 

The Company determines if a contract contains a lease based on whether it has the right to obtain substantially all of the economic benefits from the use of an identified asset which the Company does not own and whether it has the right to direct the use of an identified asset in exchange for consideration. Leased assets represent the Company’s right to use an underlying asset for the lease term and lease liabilities represent the Company’s obligation to make lease payments arising from the lease. The right-of-use asset is initially measured as the amount of the lease liability, plus any lease payments made at or before the commencement date, plus any initial direct costs incurred by the lessee, minus any lease incentives received.

  

Lease liabilities are recognized at the present value of the future lease payments at the lease commencement date. The interest rate used to determine the present value of the future lease payments is the Company’s incremental borrowing rate (“IBR”), because the interest rate implicit in most of the Company’s leases is not readily determinable.

 

The IBR is a hypothetical rate based on the Company’s understanding of what its credit rating would be to borrow and the resulting interest the Company would pay to borrow an amount equal to the lease payments in a similar economic environment over the lease term on a collateralized basis. Lease payments may be fixed or variable, however, only fixed payments or in-substance fixed payments are included in the Company’s lease liability calculation.

 

10

 

Variable lease payments are recognized in operating expenses in the period in which the obligation for those payments is incurred. The Company recognized no impairment of leased assets for the six months ended June 30, 2026 and 2025.

 

Warrant Liabilities

 

The Company accounts for the Public Warrants and Private Placement Warrants (collectively, “Warrants”), issued in connection with the merger transaction in accordance with ASC 815-40, “Derivatives and Hedging — Contracts in Entity’s Own Equity”. Such guidance provides that because the warrants do not meet the criteria for equity treatment thereunder, each warrant must be classified as a liability. Accordingly, the Company classifies each warrant as a liability at its fair value. This liability is subject to re-measurement at each balance sheet date. With each such re-measurement, the warrant liability is adjusted to fair value, with the change in fair value recognized in the Company’s consolidated statements of operations.

 

Statutory reserve

 

Pursuant to the laws applicable to Taiwan, Taiwanese entities must make appropriations from after-tax profit to the non-distributable “statutory reserve”. Subject to certain cumulative limits, the “statutory reserve” requires annual appropriations of 10% of after-tax profit until the aggregated appropriations reach 100% of the authorized capital (as determined under accounting principles generally accepted in Taiwan (“Taiwan GAAP”) at each year end). Since the YD Bio’s subsidiary in Taiwan has accumulated deficit under Taiwan GAAP during the reporting period, it is not required to make appropriations to the statutory reserve.

 

Revenue Recognition

 

The Company recognizes revenue when a customer obtains control of promised goods or receives services provided in an amount that reflects the consideration which the Company expects to receive in exchange for those goods and services. To determine revenue recognition for the arrangements that the Company determines are within the scope of ASC 606, Revenue from Contracts with Customers, the Company performs the following five steps: (1) identify the contract(s) with a customer, (2) identify the performance obligations in the contract, (3) determine the transaction price, (4) allocate the transaction price to the performance obligations in the contract and (5) recognize revenue when (or as) the entity satisfies a performance obligation.

 

The Company’s revenue from contracts with customers is derived from product revenue principally from the sales of products directly to its customers and presents revenue net of VAT.

 

Product revenue recognition — point of time

 

The performance obligations are considered to be met, and revenue is recognized when the customer obtains control of the goods. Revenue is recognized at that point in time. The customers pick up the goods directly from the Company’s premises, and the Company has satisfied the contracts’ performance obligations when the goods have been picked up, and the acceptance document has been signed by the customers. The Company does not offer sales rebates to its customers. Any discount will be net of the revenue at that point in time. The Company does not provide its customers with the right of return (except for product quality issues). The customer is required to perform a product quality check immediately upon delivery of the products and report to the Company within a few days if there is a quality issue.

  

Cost of revenue

 

Cost of revenue consists primarily of purchased costs of products for resales, the material costs and subcontracting costs of manufactured products which are directly attributable to the manufacturing of products and other costs directly related to the rendering of services performed.

 

11

 

Research and development

 

Research and development costs are expensed as incurred in accordance with ASC 730, Research and Development. The Company incurs research and development costs in the pursuit of new products and improving the formulation of existing products.

 

Shipping and handling expenses

 

The Company expenses shipping and handling expenses as incurred. The Company recorded $6,884 and $8,440 of shipping and handling expenses for the six months ended June 30, 2026 and 2025, respectively.

 

Other income, net

 

The Company has entered into leasing arrangements with corporate customers to lease equipment for the six months ended June 30, 2026 and 2025. The Company receives income from operating leases based on the fixed required rents (base rent) per the lease agreements. Rent revenue from base rents is recorded on the straight-line method, when collectability of the lease payments is deemed probable, over the terms of the related lease agreements. Operating lease revenue, as recorded on the straight-line method, in the consolidated statements of operation is recorded as other revenue. The Company recognized income from the leasing of equipment to other corporate customers of $31,318 and $31,398 for the six months ended June 30,2026 and 2025, respectively.

 

Contract liabilities

 

The Company’s contract liabilities consist of deferred revenue associated with the lease arrangements for leasing certain equipment to its customers over time and sales of goods. Deferred revenue represents amounts received or invoiced in advance of delivering goods or rendering services. These amounts are recognized as revenue when the performance obligations under the contracts are fulfilled. The table below presents the activity of the deferred revenue from the lease and sales of medical products for the six months ended June 30, 2026 and 2025, respectively:

 

    Six months
ended
June 30,
2026
    Six months
ended
June 30,
2025
 
Balance at beginning of period   $ 30,153     $ 27,568  
Advances received from customers     201,306       39,206  
Revenue recognized     (31,318 )     (31,398 )
Exchange realignment     (1,548 )     4,040  
Balance at end of period   $ 198,593     $ 39,416  

  

Stock Based Compensation

 

The Company accounts for its stock-based compensation awards in accordance with ASC Topic 718, Compensation—Stock Compensation (“ASC 718”). ASC 718 requires all stock-based payments, including grants of employee stock options, to be recognized in the statement of operations by measuring the fair value of the award on the date of grant and recognizing this fair value as stock-based compensation over the requisite service period, generally the vesting period. On July 7, 2025 the Board adopted, and the then sole shareholder of the Company approved the YD Bio Limited Equity Incentive Plan (the “Equity Incentive Plan”) to grant new awards to eligible participants from time to time, subject to and in accordance with the terms and conditions described therein. Detail awards granted and vested during six months ended June 30, 2026 see Note 14.

 

Income Taxes

 

Income taxes are accounted for under the asset and liability method in accordance with ASC 740, Income Taxes. Under this method, income tax expense is recognized for the amount of: (i) taxes payable or refundable for the current year and (ii) deferred tax consequences of temporary differences resulting from matters that have been recognized in an entity’s financial statements or tax returns

 

12

 

 

Deferred tax assets and liabilities are determined based on the temporary difference between the financial reporting and tax bases of assets and liabilities, and net operating loss and tax credit carryforwards using enacted tax rates that will be in effect for the period in which the differences are expected to reverse. The Company records a valuation allowance against the amount of deferred tax assets that it determines is not more likely than not of being realized. The effect on deferred taxes of a change in tax rates is recognized in income in the period that includes the enactment date.

 

The Company recognizes the effect of income tax positions only if those positions are more likely than not of being sustained. Recognized income tax positions are measured at the largest amount that is greater than 50% likely of being realized. Changes in recognition or measurement are reflected in the period in which the change in judgment occurs. The Company records interest related to unrecognized tax benefits and penalties, if any, within income tax expenses.

 

Retirement and other post-retirement benefits

 

Contributions to retirement accounts which are defined contribution plans are expensed in the statement of operations as and when the related employee service is provided.

 

Full time employees of the Company in Taiwan participate in a government mandated defined contribution plan, pursuant to which certain pension benefits and medical care benefits are provided to employees. Taiwanese labor regulations require that the Company make contributions to the government for these benefits based on certain percentages of the employees’ salaries, up to a maximum amount specified by the government. The Company has no legal obligation for the benefits beyond the contributions made. Total amounts of such employee benefit expenses, which were expensed as incurred, were approximately $6,679, and $3,250 for the six months ended June 30, 2026 and 2025, respectively.

 

Translation of foreign currency financial statements

 

The functional currency of YD Bio, YD Biopharma and YD USA is USD. The functional currency of Yong Ding is NTD, the local currency where it operates. The reporting currency of the Company is USD. Accordingly, the financial statements of Yong Ding are translated at the following exchange rates: assets and liabilities — current rate on balance sheet date; shareholders’ equity — historical rate; income and expenses — average rate during the period. The resulting translation adjustment is reflected in the accumulated other comprehensive income (loss).

 

Transactions denominated in currencies other than the functional currencies are recorded at the rate of exchange in effect when the transaction occurs. Gains or losses, resulting from the application of different foreign exchange rates when cash in the foreign currency is converted into the entities’ functional currency, or when foreign currency receivable and payable are settled, are credited or charged to income in the period of conversion or settlement. At period-end, the balances of foreign currency monetary assets and liabilities are recorded based on prevailing exchange rates and any resulting gains or losses are included in the consolidated statements of comprehensive income (loss).

 

Non-monetary assets and liabilities that are measured in terms of historical cost in a foreign currency are translated using the exchange rates prevailing on the transaction dates. The transaction date is the date on which the Company initially recognizes such non-monetary assets and liabilities. Non-monetary assets and liabilities that are stated at fair value are translated using the exchange rates prevailing at the dates the fair value is measured. The resulting exchange differences are recognized in accumulated other comprehensive income (loss).

 

Translation of amounts from NTD into US$ has been made at the following exchange rates for the respective years:

 

    Six months ended
June 30
    Year ended
December 31
 
    2026     2025  
Period-end NTD: US$1 exchange rate     31.85       31.34  

 

    Six months ended
June 30
 
    2026     2025  
Period average NTD: US$1 exchange rate     31.60       31.89  

 

13

 

Comprehensive (loss) income

 

Comprehensive (loss) income represents net (loss) income plus the results of certain changes in shareholders’ equity (deficit) during a period from non-owner sources.

 

Comprehensive (loss) income is defined as the changes in equity of the Company during a period from transactions and other events and circumstances excluding transactions resulting from investments by owners and distributions to owners. Among other disclosures, ASC 220, Comprehensive Income, requires that all items that are required to be recognized under current accounting standards as components of comprehensive loss be reported in a financial statement that is displayed with the same prominence as other financial statements. For each of the periods presented, the Company’s comprehensive (loss) income includes net (loss) income and foreign currency translation adjustments, which are presented in the consolidated statements of comprehensive (loss) income.

 

Net (Loss) Income per Share

 

The Company complies with accounting and disclosure requirements of FASB ASC Topic 260, “Earnings Per Share”. Basic (loss) income per share is calculated by dividing the net (loss) income by the weighted-average number of Ordinary Shares outstanding during the period. Diluted loss per share is calculated by dividing the loss by the weighted-average number of Ordinary Shares and potentially dilutive securities outstanding during the period. Potentially dilutive Ordinary Shares consist of shares issuable upon the conversion of warrants. The dilutive effect of outstanding shares is reflected in diluted earnings per share by application of the treasury stock method, or the if-converted method. The outstanding Public Warrants and Private Placement Warrants were 11,436,270 and 3,136,056 as of June 30, 2026, all of which were excluded from the calculation of diluted EPS for the six months ended June 30, 2026 because their exercise price was above the average market share price during the period. There were no outstanding warrants as of June 30, 2025. On March 31, 2026, the Company granted restricted share units (“RSUs”) to each of two directors under the Equity Incentive Plan, with each RSU representing a contingent right to receive one Ordinary Share and an aggregate target grant-date fair value of $60,000. The granted RSUs vest in four equal quarterly installments with the number of RSUs subject to vesting determined on the applicable vesting date by dividing $15,000 by the seven trading-day volume-weighted average price of the Ordinary Shares ending on the trading day immediately prior to such vesting date. As of June 30, 2026, the fair value of RSUs granted not yet vested was $30,000. The unvested RSUs has no dilutive effect on EPS.

 

Concentration of risks

 

Concentration of suppliers

 

The following suppliers accounted for 10% or more of purchase for the six months ended June 30, 2026 and 2025.

 

For the six months ended June 30, 2025, approximately 81.6% of the Company’s purchase was from Supplier A, a company that the Company’s CEO holds 12.8764%.

 

    Six months ended
June 30
 
Supplier   2026     2025  
B     42.9 %     —  
C     19.2       *  
A     —       81.6 %

 

* Represents less than 10% of purchase for the six months ended June 30, 2026 and 2025.

 

Account payable to suppliers that individually comprised 10% or more of accounts payable balances as of June 30, 2026 and December 31, 2025 are as follows:

 

Supplier   June 30,
2026
    December 31,
2025
 
D     25.8 %     —  
C     21.1 %     *  
A     —       89.5 %

 

* Represents less than 10% of accounts payable balances as of June 30, 2026 and December 31, 2025.

 

14

 

Concentration of customers

 

The following customers accounted for 10% or more of sales for the six months ended June 30, 2026 and 2025:

 

    Six months ended
June 30,
 
Customer   2026     2025  
B     48.6 %     23.3 %
A     *       29.6 %
C     —       17.2 %

 

* Represents less than 10% of revenue for the six months ended June 30, 2026 and 2025, respectively.

 

Account receivables, net from customers that individually comprised 10% or more of accounts receivable, net balances as of June 30, 2026 and December 31, 2025 are as follows:

 

Customer   June 30,
2026
    December 31,
2025
 
 A     26.9 %     30.5 %
 D     22.1 %     16.0 %
 B     17.1 %     *  
 E     *       15.6 %

 

* Represents less than 10% of accounts receivable balances as of June 30, 2026 and December 31, 2025, respectively.

 

Concentration of credit risk

 

Financial instruments that potentially expose the Company to the concentration of credit risk consist primarily of cash and cash equivalents, accounts receivable and other current assets. The Company places its cash and cash equivalents with financial institutions with credit ratings and quality where the Company considers acceptable.

 

The risks with respect to accounts receivable are mitigated by credit evaluations performed on the debtors and ongoing monitoring of outstanding balances.

 

Foreign currency exchange risk

 

The reporting currency of the Company is USD. To date the majority of the revenues and costs are denominated in NTD and a significant portion of the assets and liabilities are denominated in NTD. As a result, the Company is exposed to foreign currency exchange risk as its revenues and results of operations may be affected by fluctuations in the exchange rate between USD and NTD. If NTD depreciates against USD, the value of NTD revenues and assets as expressed in USD financial statements will decline. The Company does not hold any derivative or other financial instruments that exposes us to substantial market risk.

 

NTD is not a freely convertible currency. The Central Bank of the Republic of China, under the authority of Taiwan government, controls the conversion of NTD to foreign currencies. There are restrictions and limits on the conversion of NTD to other currencies, especially for capital account transactions. Individuals and businesses face conversion quotas and approvals required from the authorities.

 

Segment Reporting

 

The Company complies with ASU 2023-07, Segment Reporting (Topic 280): Improvements to Reportable Segment Disclosures (ASU 2023-07), which improves reportable segment disclosure requirements, primarily through enhanced disclosures about significant segment expenses among other disclosure requirements. The Company adopted ASU 2023-07 on February 6, 2024 (inception).

 

ASC Topic 280, “Segment Reporting,” requires use of the “management approach” model for segment reporting. The management approach model is based on the way a company’s chief operating decision maker (the “CODM”), which is comprised of the Company’s Chief Executive Officer and Chief Financial Officer, reviews financial information including net revenues, gross profit and total operating expenses, etc. presented on a consolidated basis for purposes of managing the business, allocating resources, making operating decisions and assessing financial performance. Reportable segments are based on products and services, geography, legal structure, management structure, or any other manner in which management disaggregates a company. See Note 21 for details.

 

15

 

Management determined that the Company’s operations constitute a single reportable segment in accordance with ASC 280. YD Bio operates exclusively in three business and industry diverse operations: 1) sales of medical devices and other related products, 2) research and development in pancreatic cancer early detection services, and 3) research and development in the sales of contact lenses.

 

All of YD Bio’s long-lived assets are mainly prepayment for property, plant, and equipment located in ROC and intangible assets related to license to patents and know-how

 

Net sales to customers by geographic area are determined by reference to the physical product shipment delivery locations requested by the customers. For example, if the products are delivered to a customer in ROC, the sales are recorded as generated in ROC; if the customer directs us to ship its products to the United States, the sales are recorded as sold in the United States.

  

Recently Issued Accounting Pronouncements Not Yet Adopted

  

In November 2024, the FASB issued ASU 2024-03, Income Statement - Reporting Comprehensive Income - Expense Disaggregation Disclosures (Subtopic 220-40): Disaggregation of Income Statement Expenses, which requires a public entity to disclose additional information about specific expense categories in the notes to the financial statements on an annual and interim basis. It is effective for fiscal years beginning after December 15, 2026, and interim periods within fiscal years beginning after December 15, 2027. In January 2025, the FASB issued ASU 2025-01 to clarify that all public entities, including non-calendar year-end entities, should adopt the disclosure requirements of ASU 2024-03. The Company is currently evaluating the impact of this standard on its consolidated financial statements and related disclosures, and do not expect the adoption will have a material impact on its financial statements and disclosures.

 

In May 2025, the FASB issued ASU 2025-04, Compensation — Stock Compensation (Topic 718) and Revenue from Contracts with Customers (Topic 606): Clarifications to Share-Based Consideration Payable to a Customer. The amendments clarify the accounting for share-based consideration payable to a customer under Topic 718 and Topic 606. The amendments are effective for annual reporting periods, including interim periods within those annual periods, beginning after December 15, 2026. Early adoption is permitted. The Company is currently evaluating the impact of this standard on its consolidated financial statements and related disclosures, and do not expect the adoption will have a material impact on its financial statements and disclosures.

 

Recently Adopted Accounting Pronouncements

 

In July 2025, the FASB issued ASU 2025-05, Financial Instruments — Credit Losses (Topic 326): Measurement of Credit Losses for Accounts Receivable and Contract Assets. The amendments provide a practical expedient and, if applicable, an accounting policy election to simplify the measurement of credit losses for certain receivables and contract assets. The amendments are effective for annual reporting periods beginning after December 15, 2025, and interim reporting periods within those annual reporting periods. Early adoption is permitted in any interim or annual period in which financial statements have not yet been issued or made available for issuance. The Company has adopted ASU 2025-05 and the adoption did not have a material impact on the Company’s unaudited consolidated financial statements.

 

Except as mentioned above, the Company does not believe other recently issued but not yet effective accounting standards, if currently adopted, would have a material effect on the Company’s consolidated balance sheets, consolidated statements of operations and comprehensive income (loss) and consolidated statements of cash flows.

 

4. ACCOUNTS RECEIVABLE

 

Accounts receivable, net consist of the following:

 

    June 30,
2026
    December 31,
2025
 
Accounts receivable   $ 234,086     $ 174,075  
Less: allowance for expected credit losses     (11,019 )     (6,598 )
Total accounts receivable, net   $ 223,067     $ 167,477  

 

Details of the changes of the expected credit loss provision are as follows:

 

16

 

   

Six months ended

June 30,

 
    2026     2025  
Beginning of the period   $ 6,598     $ 3,055  
Provision for the year     4,553       4,108  
Foreign exchange realignment     (132 )     415  
End of the period   $ 11,019     $ 7,578  

 

As of June 30, 2026 and December 31, 2025, the majority of accounts receivable is due to corporate customers with long-term relationships. The Company recognized the impairment of expected credit loss for accounts receivable of $4,553 and $4,108 for the six months ended June 30, 2026 and 2025, respectively.

 

5. INVENTORIES

 

Inventories, net consist of the following:

 

    June 30,
2026
    December 31,
2025
 
Finished goods   $ 1,891,633     $ 1,879,542  
Others     722       -  
Total     1,892,355       1,879,542  

 

The Company had no write-down of inventories for the six months ended June 30, 2026 and 2025.

 

6. PREPAID EXPENSES AND OTHER CURRENT ASSETS

 

The amount of prepaid expenses and other current assets consist of the followings:

 

    June 30,
2026
    December 31,
2025
 
Prepaid expenses   $ 397,113     $ 1,027,625  
Value added tax credit     302,160       253,246  
Others     81,036       43,145  
Total   $ 780,309     $ 1,324,016  

 

The Company did not record any expected credit loss provision for other current assets for the six months ended June 30, 2026 and 2025.

 

7. PROPERTY, PLANT AND EQUIPMENT, NET

 

Property, plant and equipment consist of the following:

 

    June 30,
2026
    December 31,
2025
 
Equipment, fixtures and furniture   $ 83,790     $ 87,916  
Less: accumulated depreciation     (33,142 )     (28,576 )
Total   $ 50,648     $ 59,340  

 

Depreciation expenses included in general and administration expenses for the six months ended June 30, 2026 and 2025 were $8,477 and $8,043 respectively. There were no impairments recognized during the six months ended June 30, 2026 and 2025.

 

17

 

8. INTANGIBLE ASSETS

 

On June 19, 2024, the Company entered into an exclusive licensed patent and know-how agreement and a supplementary agreement dated on June 28, 2024, with 3D Global Biotech Inc. (“3D Global”), a company registered in Taiwan and listed on the Taipei Stock Exchange, to acquire a global exclusive licensed patent and know-how. The Company’s CEO owns approximately 14.97% of the common shares of 3D Global at the time. The licensed patent involves the formula and technology of cell culture process, technology of cell bank construction, exosome purification, authentication technology, and exosome production which are derived from the methods of culturing human corneal limbus cells and the relevant know-how (the “3D Global Patent”). The licensed period of the 3D Global Patent is 20 years after all the relevant products are launched. In addition, the Company is obligated to pay a royalty fee of 10% of the sales of the products for 15 years on a quarterly basis and the Company is allowed to sub-license the 3D Global Patent to other third-party customers. The 3D Global Patent and know-how enables YD Biopharma to form and produce the major ingredient of its contact lens solutions and helped commence the contact lens business. The Company expects the useful life of the 3D Global Patent for the contact lens business to be 15 years. The total consideration for 3D Global Patent is $5,000,000 including VAT or $4,761,905 net of VAT. In June 2024, the Company paid $1,000,000 including VAT or $952,381 net of VAT to 3D Global for the patent, formula and know-how of the technology, which is not for use in particular research and development projects and have alternative future use. It enables the Company to provide future economic benefits from the commercial production of its contact lens business and to generate income.

 

The total research and development costs of $3,130,000 has been charged from 3D Global for the for the first through third stage of Development of LSC Cell Source, first through second stage of Establishment of LSC Master Cell Banks, first through second stage of Cell Stability Examination of LSC and the first through second and fifth stage of Raw Material Development of LSC Exosomes and the Company has paid $2,820,000 of the above amount up to June 30, 2026. As of June 30, 2026,there is no activities in progress related to the stage 4.3 to 4.4 and stage 5 stated in the following milestone table.

 

The Company will pay the remaining amounts to 3D Global for further research and development of this technology and expand the application to a variety of new eye-related drugs and products when certain conditions and milestones are satisfied and completed by 3D Global.

 

According to the 3D Global License Agreement, YD Bio is obligated to pay the following amounts in accordance with the following milestones:

 

Item   Milestones   Milestone
License Fees
(USD)
 
1. Development of corneal Limbal Stem Cell (“LSC”) Cell Source      
1   Application with Medical Center for Clinical Specimens Collection     480,000  
2   SOP Document for Technique of Separating LSC Specimens     230,000  
3   LSC Cell Analysis/Assessment Report     330,000  
2. Establishment of LSC Master Cell Banks        
1   SOP Document for LSC Amplification     230,000  
2   SOP Document for LSC Cryopreservation     280,000  
3. Cell Stability Examination of LSC        
1   Stability Examination Report of Master cell     420,000  
2   Stability Examination Report of Working cell     420,000  
4. Raw Material Development of LSC Exosomes        
1   SOP Document of Exosomes Purification Process     230,000  
2   Specification Analysis/Examination Report of Exosomes Characterization     200,000  
3   SOP Document of Mass Production Process of Exosomes Raw Material     370,000  
4   Three Batches of Trial Production Document of Exosomes Raw Material     300,000  
5   Safety Verification Report (animal testing) of Exosomes Raw Material     310,000  
5. LensMate Eye Buffer LensMate        
1   Product Consignment Development Agreement     100,000  
2   U.S. Food and Drug Administration (“FDA”) Approval for Type I Medical Material Certification     80,000  
3   Sale Certification of US OTC     20,000  

 

18

 

On June 25, 2024, the Company entered into an exclusive licensed patent and know-how agreement with EG BioMed Co., Ltd. (“EG BioMed”), a Taiwan registered company, to acquire the licensed patent of Methylation analysis technology for application in pancreatic cancer and the relevant know-how (the “EG BioMed Patent”). The Company’s CEO is a director and owned 46.16% on the date of the transaction. The Company’s CEO owns 45.3% equity interest as of June 30, 2026, and as of the date of this report. The Company is allowed to use the licensed patent and know-how in the United States for manufacturing, offering for sale, selling, using, or importing the product and providing detection services for the aforementioned purposes. The licensed period of the EG BioMed Patent is initially 10 years and automatically renews for an additional 5 years unless both parties agree not to renew, thus the useful life of the EG BioMed Patent is 15 years. The consideration for the EG BioMed Patent is NTD 60,000,000 (USD 1,830,000), and the Company is obligated to pay a royalty of 7% of the sales of the services generated from EG BioMed Patent to EG BioMed on quarterly basis. The EG BioMed Patent and know-how enabled the Company to commence its pancreatic cancer early detection service business for income generation.

 

In addition, the potential royalties due to 3D Global and EG BioMed are calculated based on 7% to 10%, respectively, of the sales of products or provision of services derived from the licensed patents in future. Therefore, they are considered variable consideration and will be recognized as cost of revenue in the income statement in the period when the related revenue occurs. The royalty expenses incurred were nil and $ 2,273 for the six months ended June 30, 2026 and 2025, respectively.

 

Intangible assets consist of the following:

 

    June 30,
2026
    December 31,
2025
 
Licensed to Patents and Know-how            
3D Global Patent   $ 970,260     $ 985,710  
EG BioMed Patent     1,884,000       1,914,000  
Less: accumulated amortization     (380,568 )     (289,971 )
Total   $ 2,473,692     $ 2,609,739  

 

Amortization expense included in general and administration expenses for the six months ended June 30, 2026 and 2025 was $95,748 and $95,142, respectively. The estimated amortization is as follows:

 

As of June 30, 2026   Estimated
amortization
expense
 
From July 1, 2026, to June 30, 2027   $ 191,496  
From July 1, 2027, to June 30, 2028     191,496  
From July 1, 2028, to June 30, 2029     191,496  
From July 1, 2029, to June 30, 2030     191,496  
From July 1, 2030, to June 30, 2031     191,496  
Thereafter     1,516,212  
Total   $ 2,473,692  

 

9. PREPAID EXPENSES, NON-CURRENT

 

On September 17, 2025, Yong Ding Biopharm Co., Ltd (Subsidiary of YD Bio) entered into a pre-sale real estate contract for the purchase of office space and parking facilities located in Taipei City, with a total contract price of $8.9 million. As of June 30, 2026 and December 31, 2025, $1.9 million and $1.4 million were prepaid for the purchase, respectively.

 

As of June 30, 2026, the remaining balance of $7.0 million is to be funded through a combination of internal cash reserves and a potential loan of up to $ 7.1 million through a designated financial institution.

 

19

 

10. LEASES

 

The Company’s operating leases consist of leases for office space. The Company is the lessee under the terms of the operating leases. For the six months ended June 30, 2026 and 2025, the operating lease cost was $10,139 and $21,695, respectively.

 

The Company’s operating leases have remaining lease terms of approximately 4 months as of June 30, 2026, and 10 months as of December 31, 2025, respectively. As of June 30, 2026, the weighted average remaining lease term and weighted average discount rate were 0.33 years and 4.22%, respectively.

 

As of June 30, 2026 and December 31, 2025, the Company stated the following amounts in the Company’s consolidated balance sheets:

 

    June 30,
2026
    December 31,
2025
 
Assets            
Right-of-use assets   $ 6,681     $ 8,470  
Total     6,681       8,470  
                 
Liabilities                
Operating lease liabilities, current     5,002       6,764  
Total lease liabilities   $ 5,002     $ 6,764  

  

Supplemental disclosure related to operating leases were as follows:

 

    June 30,
2026
    June 30,
2025
 
Cash paid for amounts included in the measurement of lease liabilities            
Operating cash flows for operating leases   $ 10,139     $ 19,187  

 

Maturities of lease liabilities were as follows:

 

As of June 30, 2026   Operating
Lease
 
From July 1, 2026, to June 30, 2027   $ 5,037  
Less: amounts representing interest     (35 )
Present Value of future minimum lease payments     5,002  
Less: Current obligations     (5,002 )
Long term obligations   $ —  

 

The Company also leased office and car park space under various short-term operating leases with the duration of less than 12 months in Taiwan. The short term leases cost was $1,273 and $1,243 for the six months ended June 30, 2026 and 2025, respectively.

 

11. ACCOUNTS PAYABLE

 

Accounts payables are non-interest bearing and generally settled within 90-day terms. All accounts payable are expected to be settled within one year. The carrying value of accounts payable are considered to be a reasonable approximation of fair value.

 

20

 

12. ACCRUED EXPENSES AND OTHER LIABILITIES

 

Accrued expenses and other liabilities consisted of the followings:

 

    June 30,
2026
    December 31,
2025
 
Accrued expenses   $ 132,424     $ 403,445  
Deferred revenue     198,593       30,153  
Other payables     2,394       4,261  
Total   $ 333,411     $ 437,859  

 

13. WARRANTS

 

As a result of the Business Combination, Breeze’s outstanding warrants were exchanged for 16,925,000 YD Bio warrants on a one-for-one basis, with the same exercise price and terms, including 11,500,000 Public Warrants and 5,425,000 Private Warrants. As of August 29, 2025, the Public Warrants began trading on the NASDAQ under the proposed symbols YDESW.

 

Public Warrants may only be exercised for a whole number of shares. No fractional shares are issued upon exercise of the Public Warrants. The Public Warrants are exercisable on the later of (a) 30 days after the consummation of a Business Combination or (b) 12 months from the closing of the Initial Public Offering. The Public Warrants will expire five years from the consummation of a Business Combination or earlier upon redemption or liquidation.

  

Once the warrants become exercisable, the Company may call the warrants for redemption:

 

  ● in whole and not in part;

 

  ● at a price of $0.01 per warrant;

 

  ● upon not less than 30 days’ prior written notice of redemption (the “30-day redemption period”) to each warrant holder; and

 

  ● if, and only if, the reported last sale price of the common stock equals or exceeds $18.00 per share for any 20 trading days within a 30-trading day period ending on the third trading day prior to the date the Company sends the notice of redemption to the warrant holders.

 

The Company may not redeem the warrants when a holder may not exercise such warrants.

 

The warrants may be exercised upon surrender of the warrant certificate on or prior to the expiration date at the offices of the warrant agent, with the exercise form on the reverse side of the warrant certificate completed and executed as indicated, accompanied by full payment of the exercise price (or on a cashless basis, if applicable), by certified or official bank check payable to the Company, for the number of warrants being exercised. The warrant holders do not have the rights or privileges of holders of common stock and any voting rights until they exercise their warrants and receive shares of common stock. After the issuance of shares of common stock upon exercise of the warrants, each holder will be entitled to one vote for each share held of record on all matters to be voted on by stockholders.

 

No fractional shares will be issued upon exercise of the warrants. If, upon exercise of the warrants, a holder would be entitled to receive a fractional interest in a share, the Company will, upon exercise, round down to the nearest whole number of shares of common stock to be issued to the warrant holder.

 

The Private Placement Warrants (including the common stock issuable upon exercise of the Private Placement Warrants) will not be transferable, assignable or salable until 30 days after the completion of the initial Business Combination and they will be non-redeemable so long as they are held by the original holders or their permitted transferees. If the Private Placement Warrants are held by someone other than the original holders or their permitted transferees, the Private Placement Warrants will be redeemable by the Company and exercisable by such holders on the same basis as the Warrants included in the Units being sold in the Initial Public Offering. Otherwise, the Private Placement Warrants have terms and provisions that are substantially identical to those of the Warrants being sold as part of the Units in the Initial Public Offering.

 

21

 

In December 2025, 62,580 public warrants were exercised and converted into ordinary shares at an exercise price of $11.5 per share, and 1,782,089 private warrants were exchanged for 205,333 ordinary shares on a cashless basis.

 

In January 2026, 1,150 public warrants were exercised and converted into ordinary shares at an exercise price of $11.5 per share, and 569,435 private warrants were exchanged for 36,773 ordinary shares on a cashless basis.

 

After the above conversion and as of June 30, 2026, there were 11,436,270 Public Warrants and 3,136,056 Private Placement Warrants outstanding. The Company classifies the outstanding Public Warrants and Private Placement Warrants as warrant liabilities on the balance sheet in accordance with the guidance contained in ASC 815-40. Under the guidance in ASC 815-40, certain warrants do not meet the criteria for equity treatment. These warrants include a clause whereby the warrant holder may be entitled to receive a net cash settlement upon the acceptance by the holders of the Company’s common stock of a tender, exchange or redemption offer. Upon such a qualifying tender cash offer (an event which could be outside the control of the Company), all Warrant holders would be entitled to cash. This factor precludes the Company from applying equity accounting as the warrant holder could receive a net cash settlement value that is greater than a holder of the Company’s common stock. Accordingly, the Company has concluded that liability accounting is required. As such, these warrants are recorded at fair value as of each reporting date with the change in fair value reported within other income in the accompanying consolidated statements of operations as “Change in fair value of warrant liability” until the warrants are exercised, expired or other facts and circumstances lead the warrant liability to be reclassified to stockholders’ equity.

 

As of June 30, 2026, the fair value of both the Company’s Private Placement Warrants and Public Warrants utilized the Company’s trading price of the Public Warrants as the terms of the Public Warrants and Private Placement Warrants are similar.

 

14. SHAREHOLDER’S EQUITY(DEFICIT)

 

Ordinary Shares — The Company is authorized to issue 500,000,000 ordinary shares with a par value of $0.0001 per share. Holders of ordinary shares are entitled to one vote per share owned on each matter properly submitted to the shareholders on which the holders of the ordinary shares are entitled to vote. The holders of ordinary shares shall be entitled to receive dividends and other distributions (payable in cash, property or capital stock of the Company) when, as and if declared thereon by our board of directors from time to time out of any assets for funds of the Company legally available therefor and shall share equally on a per share basis in such dividends and distributions.

 

As a result of the Business Combination, Breeze’s outstanding shares were exchanged for 4,140,948 ordinary shares of the Company; 64,730,411 ordinary shares of the Company were issued to the former shareholders of YD Biopharma.

 

In addition, on August 28, 2025, the Company issued 1,650,000 ordinary shares to certain investors in connection with a PIPE Financing raising aggregate proceeds of $13.2 million at a price per share of $8.00.

 

In December 2025, 62,580 public warrants were exercised and converted into ordinary shares at an exercise price of $11.5 per share, and 1,782,089 private warrants were exchanged for 205,333 ordinary shares on a cashless basis.

 

In January 2026, 1,150 public warrants were exercised and converted into ordinary shares at an exercise price of $11.5 per share, and 569,435 private warrants were exchanged for 36,773 ordinary shares on a cashless basis.

 

On July 7, 2025 the Board adopted, and the then sole shareholder of the Company approved the YD Bio Limited Equity Incentive Plan (the “Equity Incentive Plan”). The Equity Incentive Plan is adopted by the Company in connection with the Business Combination. From and after the time of the Business Combination, the Company intends to use this Equity Incentive Plan to grant new awards to eligible participants from time to time, subject to and in accordance with the terms and conditions described therein. As of December 31, 2025, no awards have been granted under the plan.

 

On March 31, 2026, the Company granted restricted share units (“RSUs”) to each of two directors under the Equity Incentive Plan, with each RSU representing a contingent right to receive one Ordinary Share and an aggregate target grant-date fair value of $60,000. The granted RSUs vest in four equal quarterly installments with the number of RSUs subject to vesting determined on the applicable vesting date by dividing $15,000 by the seven trading-day volume-weighted average price of the Ordinary Shares ending on the trading day immediately prior to such vesting date. Upon the vesting of certain RSUs, the Company issued 2,081 Ordinary Shares to each of the two directors on March 31, 2026 and 5,749 Ordinary Shares to each of the two directors on June 30, 2026.

 

After the above conversion and as of June 30, 2026, there were 70,842,844 ordinary shares outstanding.

 

22

 

15. FAIR VALUE MEASUREMENTS

 

The following table presents information about the Company’s financial liabilities that are measured at fair value on a recurring basis as of June 30, 2026 and December 31,2025, and indicates the fair value hierarchy of the valuation inputs the Company utilized to determine such fair value.

 

    June 30, 2026  
Description   Level 1     Level 2     Level 3  
Liabilities                        
Warrant liability - Public Warrants   $ 3,545,244     $ —     $ —  
Warrant liability - Private Placement Warrants   $ 972,177     $ —     $ —  

 

    December 31, 2025  
Description   Level 1     Level 2     Level 3  
Liabilities                        
Warrant liability - Public Warrants   $ 11,323,046     $ —     $ —  
Warrant liability - Private Placement Warrants   $ 3,668,436     $ —     $ —  

 

As of June 30, 2026 and December 31, 2025, the fair value of both the Company’s Private Placement Warrants and Public Warrants utilized the Company’s trading price of the Public Warrants as the terms of the Public Warrants and Private Placement Warrants are similar. The measurement of Warrants is classified as Level 1 due to the use of an observable market quote in an active market under the ticker YDESW. The quoted prices of the Public Warrants were $0.31 and $0.99 per warrant as of June 30, 2026 and December 31, 2025, respectively.

 

The following table presents the changes in the fair value of warrant liabilities for the six months ended June 30, 2026:

 

    Private
Placement
    Public     Warrant
Liabilities
 
Fair value as of December 31, 2025   $ 3,668,436     $ 11,323,046     $ 14,991,482  
Warrants exercised for common shares     (626,379 )     (1,150 )     (627,529 )
Change in fair value of warrant liabilities     (2,069,880 )     (7,776,652 )     (9,846,532 )
Fair value as of June 30, 2026   $ 972,177     $ 3,545,244     $ 4,517,421  

  

16. REVENUE

 

For the six months ended June 30, 2026 and 2025, the Company’s revenue was all recognized at point of time.

 

Revenue for the six months ended June 30, 2026, consists of the following:

 

    Corporate
Customers
    Retail
Customers
    Total  
Drugs   $ 500,537     $ 15,735     $ 516,272  
Medical and related products     239,498       382       239,880  
Service     66,642       -       66,642  
Beauty products     11,988       1,375       13,363  
Nutritional products     4,716       1,077       5,793  
Supplements     3,498       1,053       4,551  
Total   $ 826,879     $ 19,622     $ 846,501  

 

 

23

 

The Company operates in multiple geographic regions. Net revenues by geographic area for the period are as follows:

 

Net Revenues by Geographic Area

 

Geographic Area   Net
Revenues
 
United States   $ 66,642  
Taiwan     779,859  
Total   $ 846,501  

 

The United States revenues are derived from technical services provided, while all other product categories, including drugs, medical and related products, nutritional products, and supplements, are sold in Taiwan.

 

Revenue for the six months ended June 30, 2025, consists of the following:

 

    Corporate
Customers
    Retail
Customers
    Total  
Drugs   $ 90,210     $ —     $ 90,210  
Medical and related products     75,966       32       75,998  
Contact lenses     35,000       —       35,000  
Nutritional products     2,368       —       2,368  
Supplements     431       —       431  
Total   $ 203,975     $ 32     $ 204,007  

 

The Company operates in multiple geographic regions. Net revenues by geographic area for the period are as follows:

 

Net Revenues by Geographic Area

 

Geographic Area   Net
Revenues
 
United States   $ 35,000  
Taiwan     169,007  
Total   $ 204,007  

 

The United States revenues are derived from contact lens sales, while all other product categories, including drugs, medical and related products, nutritional products, and supplements, are sold in Taiwan.

 

17. RESEARCH AND DEVELOPMENT EXPENSES

 

For the six months ended June 30, 2026 and 2025, the Company incurred research and development expenses primarily with related parties.

 

In June 2024, the Company entered into an exclusive license agreement with 3D Global Biotech Inc. (a related party in which the CEO holds approximately 12.8764% equity interest) for global patent and know-how related to contact lens technology for a total consideration of $5,000,000 (including VAT). In June 2024, the Company paid $1,000,000 including VAT or $952,381 net of VAT to 3D Global for the patent, formula and know-how of the technology. The Company is also obligated to pay a royalty of 10% of the sales of the products generated from 3D Global Patent to 3D Global on a quarterly basis.

 

For the six months ended June 30, 2026 and 2025, the Company recorded $1,160,000 and $790,000 (including VAT), respectively as research and development costs charged from 3D Global.

 

In June 2024, the Company licensed methylation analysis technology for pancreatic cancer from EG BioMed Co., Ltd. (a related party in which the CEO is a director and holds 45.3% equity interest) for NTD 60,000,000 ($1,830,000), and the Company is obligated to pay a royalty of 7% of sales generated from the EG BioMed Patent to EG BioMed on a quarterly basis.

 

For the six months ended June 30, 2026 and 2025, the Company incurred nil and $16,071, respectively, for the research and development expenses for the pancreatic cancer early detection service licensed patent and $3,889 and nil, respectively, for the research and development expenses for the Breast Cancer Patent.

 

As of June 30, 2026, the Company has not capitalized any development cost.

 

24

 

18. INCOME TAXES

 

YD Bio and YD Biopharma are incorporated in the Cayman Islands, which is exempt from income tax. YD Biopharma’s 100% wholly owned subsidiary, Yong Ding, is incorporated in the ROC and is subject to the ROC Income Tax Law. The applicable tax rate is 20% for the six months ended June 30, 2026 and 2025. YD USA is a company incorporated in the state of Delaware and operating in Washington, USA, subject to federal income tax at a rate of 21%, with no state income tax.

 

Significant components of the provision for income taxes (benefits) are as follows:

 

    Six months ended June 30,  
    2026     2025  
Current tax   $ —     $ —  
Deferred tax – tax loss     —       —  
Deferred tax – book-tax difference     —       (1,507 )
Income taxes (benefits) expenses   $ —     $ (1,507 )

 

Reconciliation of the differences between the Income Tax rate applicable to profits and the income tax (benefits) expenses of the Company:

 

    Six months ended June 30,  
    2026     2025  
Income(loss) before taxation   $ 6,700,497     $ (1,918,088 )
                 
Notional tax on loss before tax                
Computed expected tax (benefits) expense     (242,555 )     (383,618 )
Non-taxable or non-deductible expenses     (2,213 )     165,660  
Foreign rate differences     23,667       (511 )
Change in valuation allowances     221,101       216,962  
Total   $ —     $ (1,507 )

  

The following table reconciles statutory rate of jurisdictions in which we do business to Yong Ding’s effective tax rate:

 

    Six months ended June 30,  
    2026     2025  
Statutory income tax rate     20.00 %     20.00 %
Non-taxable or non-deductible expenses     0.19 %     0.01 %
Change in valuation allowances     -20.19 %     -19.86 %
Effective tax rate     0.00 %     0.15 %

 

The following table reconciles statutory rate of jurisdictions in which we do business to YD USA’s effective tax rate:

 

    Six months ended June 30,  
    2026     2025  
Statutory income tax rate     21.00 %     20.00 %
Non-taxable or non-deductible expenses     0.00 %     0.00 %
Foreign rate differences     0.00 %     1.00 %
Change in valuation allowances     -21.00 %     -21.00 %
Effective tax rate     0.00 %     0.00 %

 

25

 

Deferred tax assets are as follows:

 

    June 30,
2026
    December 31,
2025
 
Deferred tax assets                
Tax losses carry forwards   $ 771,772     $ 551,303  
Expected credit losses     2,174       1,543  
Others     —       —  
Valuation allowance     (773,946 )     (552,846 )
    $ —     $ —  
                 
Total deferred tax assets   $ —     $ —  

 

The Company has recognized deferred tax assets for these loss carryforwards. However, it is not probable that future taxable income will be sufficient to realize the benefits, the Company has established a full valuation allowance against the entire amount of such deferred tax assets.

 

As of June 30, 2026, Yong Ding had net operating loss carryforwards of $3,883,438. The carry forward losses of $732,880, $ 1,972,302 and $ 1,178,256 will expire in 2034, 2035 and 2036, respectively, if not utilized.

 

As of June 30, 2026, YD USA had federal net operating loss carryforwards of $187,768, which may be carried forward indefinitely to offset future taxable income, but are subject to the 80% taxable income limitation upon utilization.

 

19. COMMITMENTS AND CONTINGENCIES

 

As of June 30, 2026 and through the date of this report, there are no pending legal proceedings to which the Company or its subsidiaries are a party, nor is the Company aware of any threatened litigation that could reasonably be expected to have a material adverse effect on its business, financial condition, or results of operations.

 

According to the agreement entered into with 3D Global in June 2024 with respect to the 3D Global Patent, the Company is obligated to pay up to $4 million when certain conditions and milestones are satisfied and completed by 3D Global.

 

On September 17, 2025, Yong Ding Biopharm Co., Ltd (Subsidiary of YD Bio) entered into a pre-sale real estate contract for the purchase of office space and parking facilities located in Taipei City. The contract covers an office unit and four statutory parking spaces with a total contract price of US$8,890,625 (NT$284,500,000, converted at an exchange rate of approximately 32 NT$/US$).

 

As of June 30, 2026, the remaining balance of $6,934,062 (NT$221,890,000) is to be funded through a combination of internal cash reserves and a potential loan of up to US$ 7,112,500 (NT$ 227,600,000) through a designated financial institution.

  

20. RELATED PARTY TRANSACTIONS

  

As of June 30, 2026, amounts due from affiliates consisted of the following:

 

Name   Amount     Relationship   Note
3D Global   $ 33,636     The Company’s CEO, the director of YD Biopharma, holds 12.8764% of 3D Global shares   Prepaid royalty fee

 

As of December 31, 2025, amounts due from affiliates consisted of the following:

 

Name   Amount     Relationship   Note
3D Global   $ 33,636     The Company’s CEO, the director of YD Biopharma, holds 12.8764% of 3D Global shares   Prepaid royalty fee
EG BioMed   $ 291,540     The Company’s CEO, the director of the Company, holds 45.3% of the shares of EG BioMed   Prepayment of research and development expenses and other expenses

 

26

 

As of June 30, 2026, the amounts due to affiliates consisted of the following:

 

Name   Amount     Relationship   Note
3D Global   $ 310,000     The Company’s CEO, the director of YD Biopharma, holds 12.8764% of 3D Global shares   Research and development expenses payable
EG Bio USA   $ 45,000     EG Bio USA is a wholly owned subsidiary of EG BioMed   Rental expenses and service charge for laboratory payable
EG BioMed   $ 3,864     The Company’s CEO, the director of Company, holds 45.3% of the shares of EG BioMed   Research and development expenses payable

 

As of December 31, 2025, the amounts due to affiliates consisted of the following:

 

Name   Amount     Relationship   Note
3D Global   $ 350,400     The Company’s CEO, the director of YD Biopharma, holds 12.8764% of 3D Global shares   Trade payables of the Company, interest free and payment on demand
3D Global   $ 420,429     The Company’s CEO, the director of YD Biopharma, holds 12.8764% of 3D Global shares   Research and development expenses payable
EG Bio USA   $ 48,471     EG Bio USA is a wholly owned subsidiary of EG BioMed   Rental expenses and service charge for laboratory payable

  

During the six months ended June 30, 2026, the Company had the following transactions with affiliates:

 

Name   Amount     Relationship   Note
3D Global   $ 1,104,877     The Company’s CEO, the director of Company, holds 12.8764% of the shares of 3D Global   Research and development expenses
EG BioMed   $ 3,889     The Company’s CEO, the director of Company, holds 45.3% of the shares of EG BioMed   Research and development expenses
EG Bio USA   $ 90,000     EG Bio USA is a wholly-owned subsidiary of EG BioMed   Rental expenses and service charge for laboratory

 

During the six months ended June 30, 2025, the Company had the following transactions with affiliates:

 

Name   Amount     Relationship   Note
3D Global   $ 775,318     The Company’s CEO, the director of Company, holds 12.8764% of the shares of 3D Global   Research and development expenses
3D Global   $ 359,091     The Company’s CEO, the director of Company, holds 12.8764% of the shares of 3D Global   Products transaction
3D Global   $ 2,273     The Company’s CEO, the director of Company, holds 12.8764% of the shares of 3D Global   Royalties
EG BioMed   $ 16,071     The Company’s CEO, the director of Company, holds 45.3% of the shares of EG BioMed   Research and development expenses
EG Bio USA   $ 45,000     EG Bio USA is a wholly-owned subsidiary of EG BioMed   Rental expenses and service charge for laboratory

 

27

 

21. SEGMENT REPORTING

 

The Company’s chief operating decision maker evaluates segment performance and allocates resources based on several factors, of which the primary financial measure is operating income.

 

The Company acquired the 3D Global Patent and EG BioMed Patent in June 2024 and commenced the pancreatic cancer early detection service and sales of contact lens business. For the six months ended June 30, 2026 and 2025, revenue of nil and $35,000 was generated from 3D Global Patent.

 

The Company primarily operates in the ROC and substantially all of the Company’s long-lived assets are located in the ROC. The Company provides Laboratory Developed Test (LDT) services to healthcare professionals across the United States.

  

The Company operates in a single reportable segment. The Company’s Chief Operating Decision Maker allocates resources and evaluates performance based on financial information presented on a consolidated basis. In accordance with ASU 2023-07, the significant expense categories regularly provided to and reviewed by the CODM on a consolidated basis include cost of revenues and operating expenses. The Company's revenue-generating activities are derived from several distinct product and service lines. Entity-wide disaggregated net revenues and direct costs for these lines for the six months ended June 30, 2026 and 2025 were as follows:

 

For six months ended June 30, 2026   Sales of medical
and other
related products
    Research and
development of
pancreatic
cancer early
detection
services
    Research and
development of
sales of contact
lenses
    Corporate
unallocated
    Consolidated  
Net revenues   $ 779,859     $ -     $ -     $ 66,642     $ 846,501  
Cost of revenues     (578,271 )     -       -       -       (578,271 )
Gross profit     201,588       -       -       66,642       268,230  
Total operating expenses     (239,849 )     (63,200 )     (1,243,747 )     (1,956,090 )     (3,502,886 )
Operating loss     (38,261 )     (63,200 )     (1,243,747 )     (1,889,448 )     (3,234,656 )
Finance income, net     35,742       -       -       16,963       52,705  
Other income (expenses), net     35,922       -       -       (6 )     35,916  
Change in fair value of warrant liabilities     -       -       -       9,846,532       9,846,532  
Net loss     33,403       (63,200 )     (1,243,747 )     7,974,041       6,700,497  
                                         
As of June 30, 2026                                        
Identifiable long-lived assets     1,995,198       1,632,800       840,892       -       4,468,890  
Total assets   $ 4,233,357     $ 1,632,800     $ 840,892     $ 3,353,212     $ 10,060,261  

 

For six months ended June 30, 2025   Sales of medical
and other
related products
    Research and
development of
pancreatic
cancer early
detection
services
    Research and
development of
sales of contact
lenses
    Corporate
unallocated
    Consolidated  
Net revenues   $ 169,007     $ —     $ 35,000     $ —     $ 204,007  
Cost of revenues     (109,342 )     —       (25,870 )     —       (135,212 )
Gross profit     59,665       —       9,130       —       68,795  
Total operating expenses     (268,734 )     (16,071 )     (835,564 )     (902,258 )     (2,022,627 )
Operating loss     (209,069 )     (16,071 )     (826,434 )     (902,258 )     (1,953,832 )
Finance income, net     17,108       —       —       1,421       18,439  
Other income (expenses), net     17,305       —       —       —       17,305  
Income tax expenses     (1,507 )     —       —       —       (1,507 )
Net loss     (173,239 )     (16,071 )     (826,434 )     (900,837 )     (1,916,581 )
                                         
As of June 30, 2025                                        
Identifiable long-lived assets     83,827       1,915,200       986,328       —       2,985,355  
Total assets   $ 934,288     $ 1,915,200     $ 1,464,966     $ 1,526,632     $ 5,841,086  

 

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