Data / Medical devices / Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented / Germany
FDA-registered makers of Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented in Germany: 8 establishments
8 establishments in Germany are registered with the FDA to make Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented (product code KWS). 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, Shoulder, Semi-Constrained, Metal/Polymer Cemented
- Product code
- KWS
- Country
- Germany
Makers of Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Arthrex GmbH | Munich Bavaria, Germany | Exporter to the US, Specification developer | 11 | June 7, 2021 | 0 | 0 | 0 | api.fda.gov |
| Friedrich Daniels GMBH | SOLINGEN North Rhine-Westphalia, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GB Implantat Technologie GMBH | Bochum North Rhine-Westphalia, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kammerer Medical Systems GmbH & Co. KG | Stockach Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Osartis GMBH | Muenster Hesse, Germany | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tontarra Medizintechnik GMBH | WURMLINGEN Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| W+S Solutions GMBH | Tuttlingen Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Waldemar Link GmbH & Co. KG | Norderstedt Schleswig-Holstein, Germany | 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.