Changes in Beneficial Ownership · 4
Femasys Inc.
FEMYNASDAQEQUITYCurrent
Changes in Beneficial Ownership
Structured filing — 4
ownership.xml
Filing details
- Report period
- 2026-03-17
- Issuer
- FEMASYS INC
- Issuer CIK
- 0001339005
- Trading symbol
- FEMY
- No longer subject to Section 16
- Checked
Reporting owner 1
- Name
- PharmaCyte Biotech, Inc.
- Reporting owner CIK
- 0001157075
- Relationship
- 10% owner
- Address
- 3960 HOWARD HUGHES PARKWAY, SUITE 500, LAS VEGAS, NV, 89169
Remarks
The Reporting Person's beneficial ownership has fallen below ten percent. As a result, the Reporting Person is no longer subject to Section 16 in connection with its transactions in the equity securities of the Issuer and therefore will no longer report any such transactions on Form 4 or Form 5.
Signature 1
- Signed
- /s/ Joshua N. Silverman, President and CEO
- Date
- 2026-03-18
Company context
We are a leading biomedical innovator, addressing significant unmet needs in women’s health worldwide, with a broad patent-protected portfolio of disruptive, accessible, in-office therapeutic and diagnostic products. We are a U.S. manufacturer that has received global regulatory approvals for its product portfolio worldwide, and its products are currently being commercialized in the U.S. and key international markets. FemaSeed® Intratubal Insemination, a groundbreaking infertility treatment delivering sperm directly to the site of conception, is U.S. FDA-cleared and approved in Europe, United Kingdom (“UK”), Canada, Israel, Australia and New Zealand. A peer-reviewed publication of positive data from its pivotal clinical trial of FemaSeed demonstrated effectiveness and safety with high satisfaction from both patients and practitioners. In August 2025, we announced the introduction of its FemSperm™ Setup Kit, the first in a planned family of products designed to fully enable gynecologists for FemaSeed Intratubal Insemination. The setup kit includes customized components, such as a pre-configured centrifuge to optimize sperm preparation for use with FemaSeed. FemVue®, a companion diagnostic for fallopian tube assessment via ultrasound, is U.S. FDA-cleared and approved in Europe, UK, Canada, Japan, Israel, Australia and New Zealand. FemCerv®, an endocervical tissue sampler for cervical cancer diagnosis, is U.S. FDA-cleared and approved in Europe, UK, Canada, Israel and New Zealan