Data / Medical devices / Instruments, Dental Hand / Switzerland
FDA-registered makers of Instruments, Dental Hand in Switzerland: 6 establishments
6 establishments in Switzerland are registered with the FDA to make Instruments, Dental Hand (product code DZN). 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
- Instruments, Dental Hand
- Product code
- DZN
- Country
- Switzerland
Makers of Instruments, Dental Hand in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Polydentia S.A. | MEZZOVICO-Vira Ticino, Switzerland | Manufacturer, Repackager or relabeler | 1 | January 17, 1980 | 0 | 0 | 0 | api.fda.gov |
| Cendres+metaux SA | Biel/Bienne Bern, Switzerland | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| FKG Dentaire Sarl | LE CRET-DU-LOCLE Neuchatel, Switzerland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gebruder Renggli, AG | Schaffhausen, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smile Line SA | St-Imier Bern, Switzerland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| medmix Switzerland AG | Haag 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.