Data / Medical devices / Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented / Switzerland
FDA-registered makers of Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented in Switzerland: 8 establishments
8 establishments in Switzerland are registered with the FDA to make Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented (product code KWY). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
- Product code
- KWY
- Country
- Switzerland
Makers of Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Zimmer GMBH | WINTERTHUR Zurich, Switzerland | Contract manufacturer, Manufacturer | 2 | November 5, 2019 | 0 | 0 | 0 | api.fda.gov |
| Medacta International SA | Castel San Pietro Ticino, Switzerland | Complaint file establishment, Manufacturer, Specification developer | 1 | March 2, 2010 | 0 | 0 | 0 | api.fda.gov |
| Medacta International SA | Rancate Ticino, Switzerland | Complaint file establishment, Manufacturer | 1 | March 2, 2010 | 0 | 0 | 0 | api.fda.gov |
| Smith & Nephew Orthopaedics AG | AARAU Aargau, Switzerland | Manufacturer | 1 | January 23, 2003 | 0 | 0 | 0 | api.fda.gov |
| Baechler Feintech AG | Hoelstein Basel-Landschaft, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Frueh Verpackungstechnik AG | Fehraltorf Zurich, 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 | |
| Ortek AG | MERENSCHWAND Aargau, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.