Data / Medical devices / Fastener, Fixation, Biodegradable, Soft Tissue / Switzerland
FDA-registered makers of Fastener, Fixation, Biodegradable, Soft Tissue in Switzerland: 7 establishments
7 establishments in Switzerland are registered with the FDA to make Fastener, Fixation, Biodegradable, Soft Tissue (product code MAI). 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
- Fastener, Fixation, Biodegradable, Soft Tissue
- Product code
- MAI
- Country
- Switzerland
Makers of Fastener, Fixation, Biodegradable, Soft Tissue in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Medos International Sarl | Le Locle Neuchatel, Switzerland | Specification developer | 21 | February 5, 2025 | 0 | 0 | 0 | api.fda.gov |
| Medacta International SA | Castel San Pietro Ticino, Switzerland | Complaint file establishment, Exporter to the US, Manufacturer | 5 | September 18, 2023 | 0 | 0 | 0 | api.fda.gov |
| Medacta International SA | Rancate Ticino, Switzerland | Complaint file establishment, Exporter to the US, Manufacturer | 5 | September 18, 2023 | 0 | 0 | 0 | api.fda.gov |
| SURGICAL FUSION TECHNOLOGIES GmbH | Schlieren Zurich, Switzerland | Specification developer | 2 | April 1, 2024 | 0 | 0 | 0 | api.fda.gov |
| Maillefer Instruments Holding Sarl | BALLAIGUES Vaud, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ruetschi Technology SA | Yverdon-les-Bains Vaud, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Samaplast AG | Sankt Margrethen Sankt Gallen, 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.