Data / Medical devices / United Kingdom / THE FEMALE HEALTH COMPANY (UK) Plc
THE FEMALE HEALTH COMPANY (UK) Plc: FDA-registered device maker in LONDON London, City of, United Kingdom, 1 PMA approval
THE FEMALE HEALTH COMPANY (UK) Plc is registered with the FDA (registration 8044101) in LONDON London, City of, United Kingdom. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated March 10, 2009. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 8044101
- FEI number
- 3006633332
- Address
- Unit 23 Park Royal Metro Centre Britannia Way, LONDON London, City of, United Kingdom, NW10 7PA
- Owner or operator
- Clear Future, Inc. (10092736)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- February 12, 2025
- Registered through
- 2026
- Brand names listed
- FC2 Female Condom
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Single-Use Internal Condom | MBU | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| March 10, 2009 | P080002 | FC2 FEMALE CONDOM | MBU | 2 | June 23, 2017 | accessdata.fda.gov |
Updated June 23, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.