Data / Medical devices / Fastener, Fixation, Nondegradable, Soft Tissue / Switzerland
FDA-registered makers of Fastener, Fixation, Nondegradable, Soft Tissue in Switzerland: 8 establishments
8 establishments in Switzerland are registered with the FDA to make Fastener, Fixation, Nondegradable, Soft Tissue (product code MBI). 5 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, Nondegradable, Soft Tissue
- Product code
- MBI
- Country
- Switzerland
Makers of Fastener, Fixation, Nondegradable, Soft Tissue 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, Exporter to the US, Manufacturer | 42 | July 1, 2025 | 0 | 0 | 0 | api.fda.gov |
| Medacta International SA | Rancate Ticino, Switzerland | Complaint file establishment, Exporter to the US, Manufacturer | 42 | July 1, 2025 | 0 | 0 | 0 | api.fda.gov |
| Medos International Sarl | Le Locle Neuchatel, Switzerland | Specification developer | 16 | October 6, 2023 | 0 | 0 | 0 | api.fda.gov |
| Synthes GMBH | Zuchwil Solothurn, Switzerland | Specification developer | 1 | March 15, 2000 | 0 | 0 | 0 | api.fda.gov |
| Synthes GMBH | Selzach Solothurn, Switzerland | Manufacturer | 1 | March 15, 2000 | 0 | 0 | 0 | api.fda.gov |
| Jabil Switzerland Manufacturing GmbH (Mezzovico) | Mezzovico Ticino, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medartis AG | BASEL Basel-Stadt, Switzerland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zimmer GMBH | WINTERTHUR Zurich, Switzerland | 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.