Data / Medical devices / Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented / France
FDA-registered makers of Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented in France: 8 establishments
8 establishments in France are registered with the FDA to make Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented (product code LPH). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- Product code
- LPH
- Country
- France
Makers of Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Serf | DECINES CHARPIEU Rhone, France | Manufacturer | 1 | July 25, 2025 | 0 | 0 | 0 | api.fda.gov |
| Biomet France | Valence Drome, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Marle Finishing SAS | La Talaudiere Loire, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Conteneur SAS | SAINT-SOUPPLETS Seine-et-Marne, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Precera Medical Herouville SAS | HEROUVILLE ST CLAIR CEDEX Normandie, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SAS Etablissements Maurice Marle | NOGENT Haute-Marne, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sferic | MENARS Centre-Val de Loire, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Westlake Plastics Europe | TOURCOING Nord, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.