Data / Medical devices / United States / Femmepharma Consumer HC, LLC
Femmepharma Consumer HC, LLC: FDA-registered device maker in Wayne, PA, United States, 1 510(k) clearance
Femmepharma Consumer HC, LLC is registered with the FDA (registration 3016931143) in Wayne, PA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 13, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016931143
- Address
- 175 Strafford Ave BLDG 4 Suite 275, Wayne, PA, United States, 19087
- Owner or operator
- FemmePharma Consumer HC, LLC (10074732)
- Roles
- Specification developer
- First device listed
- May 29, 2020
- Registered through
- 2026
- Brand names listed
- FemmePharma, Mia Vita, Satisfaite
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lubricant, Personal | NUC | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 13, 2019 | K190752 | Satisfaite | NUC | Substantially Equivalent | Femmepharma Consumer Healthcare, LLC | accessdata.fda.gov |
Compare with other makers
Updated December 13, 2019. 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.