Data / Medical devices / Shoulder Prosthesis, Reverse Configuration / France
FDA-registered makers of Shoulder Prosthesis, Reverse Configuration in France: 12 establishments
12 establishments in France are registered with the FDA to make Shoulder Prosthesis, Reverse Configuration (product code PHX). 5 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Shoulder Prosthesis, Reverse Configuration
- Product code
- PHX
- Country
- France
Makers of Shoulder Prosthesis, Reverse Configuration in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Tornier S.A.S. | Montbonnot Saint-Martin Isere, France | Complaint file establishment, Contract manufacturer, Exporter to the US, Manufacturer, Specification developer | 18 | April 3, 2026 | 0 | 2 | 0 | api.fda.gov |
| Fx Shoulder Solutions SAS | Viriat Auvergne-Rhone-Alpes, France | Complaint file establishment, Manufacturer, Specification developer | 12 | May 15, 2024 | 0 | 0 | 0 | api.fda.gov |
| FH Industrie | QUIMPER Finistere, France | Manufacturer | 10 | January 9, 2026 | 0 | 0 | 0 | api.fda.gov |
| Tornier S.A.S | Montbonnot Saint-Martin Isere, France | Manufacturer | 8 | February 21, 2024 | 0 | 0 | 0 | api.fda.gov |
| Imascap | PLOUZANE Finistere, France | Specification developer | 3 | April 3, 2026 | 0 | 0 | 0 | api.fda.gov |
| Cefimeca | La Talaudiere Loire, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Group | SAINT-PRIEST Auvergne-Rhone-Alpes, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Precimade | Bourg en Bresse Ain, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Simon SAS | Bayeux Calvados, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Symmetry Medical Polyvac SAS | WAMBRECHIES Nord, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Viant Chaumont S.A.S. | CHAUMONT Haute-Marne, 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.