Data / Medical devices / Shoulder Prosthesis, Reverse Configuration / Switzerland
FDA-registered makers of Shoulder Prosthesis, Reverse Configuration in Switzerland: 9 establishments
9 establishments in Switzerland are registered with the FDA to make Shoulder Prosthesis, Reverse Configuration (product code PHX). 4 have 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
- Shoulder Prosthesis, Reverse Configuration
- Product code
- PHX
- Country
- Switzerland
Makers of Shoulder Prosthesis, Reverse Configuration in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Medacta International SA | Castel San Pietro Ticino, Switzerland | Complaint file establishment, Manufacturer | 14 | June 10, 2026 | 0 | 0 | 0 | api.fda.gov |
| Medacta International SA | Rancate Ticino, Switzerland | Complaint file establishment, Manufacturer | 14 | June 10, 2026 | 0 | 0 | 0 | api.fda.gov |
| Zimmer GMBH | WINTERTHUR Zurich, Switzerland | Manufacturer | 4 | January 29, 2020 | 0 | 0 | 0 | api.fda.gov |
| STRYKER GmbH | SELZACH Solothurn, Switzerland | Complaint file establishment, Specification developer | 1 | December 27, 2013 | 0 | 0 | 0 | api.fda.gov |
| Baechler Feintech AG | Hoelstein Basel-Landschaft, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Innotool&greminger AG | Erlen Thurgau, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Moser-Baer AG | Sumiswald Bern, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Spitrex Orthopedics Switzerland SA | Le Locle Neuchatel, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SQ Products AG | Inwil Luzern, Switzerland | 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.