Data / Medical devices / United States / Femcap.inc
Femcap.inc: FDA-registered device maker in Warren, MI, United States, 1 PMA approval
Femcap.inc is registered with the FDA (registration 3002764647) in Warren, MI, United States. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated March 28, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3002764647
- Address
- 23290 Schoenherr Rd, Warren, MI, United States, 48089
- Owner or operator
- FemCap Inc. (10086045)
- Roles
- Manufacturer
- First device listed
- October 12, 2022
- Registered through
- 2026
- Brand names listed
- FemCap
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cap, Cervical, Contraceptive | LLQ | 3 | Manufacturer | 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 28, 2003 | P020041 | FEMCAP BARRIER CONTRACEPTIVE | LLQ | 3 | August 21, 2013 | accessdata.fda.gov |
Updated August 21, 2013. 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.