Data / Medical devices / Screw, Fixation, Intraosseous / Switzerland
FDA-registered makers of Screw, Fixation, Intraosseous in Switzerland: 6 establishments
6 establishments in Switzerland are registered with the FDA to make Screw, Fixation, Intraosseous (product code DZL). 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
- Screw, Fixation, Intraosseous
- Product code
- DZL
- Country
- Switzerland
Makers of Screw, Fixation, Intraosseous in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Synthes GMBH | Zuchwil Solothurn, Switzerland | Specification developer | 11 | April 6, 2005 | 0 | 0 | 0 | api.fda.gov |
| Synthes GMBH | Selzach Solothurn, Switzerland | Manufacturer | 3 | May 18, 2001 | 0 | 0 | 0 | api.fda.gov |
| Institut Straumann AG | BASEL Basel-Stadt, Switzerland | Specification developer | 2 | April 5, 2005 | 0 | 0 | 0 | api.fda.gov |
| Straumann Villeret SA | VILLERET Bern, Switzerland | Manufacturer | 2 | April 5, 2005 | 0 | 0 | 0 | api.fda.gov |
| Jabil Switzerland Manufacturing GmbH (Balsthal) | Balsthal Solothurn, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jabil Switzerland Manufacturing GmbH (Mezzovico) | Mezzovico Ticino, 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.