Data / Medical devices / France / Womed SAS
Womed SAS: FDA-registered device maker in Montpellier Herault, France, 1 PMA approval
Womed SAS is registered with the FDA (registration 3031365458) in Montpellier Herault, France. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated September 9, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3031365458
- Address
- 1919 route de mende Batiment Balard CIT, Montpellier Herault, France, 34090
- Owner or operator
- WOMED SAS (10094451)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- December 2, 2025
- Registered through
- 2026
- Brand names listed
- Womed Leaf
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Barrier, Absorbable, Adhesion | MCN | 3 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| September 9, 2025 | P240015 | Womed Leaf Resorbable Adhesion Barrier | MCN | 3 | October 25, 2026 | accessdata.fda.gov |
Compare with other makers
Updated October 25, 2026. 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.