Data / Medical devices / Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece / Switzerland
FDA-registered makers of Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece in Switzerland: 9 establishments
9 establishments in Switzerland are registered with the FDA to make Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece (product code ERL). 2 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
- Product code
- ERL
- Country
- Switzerland
Makers of Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bien-Air Surgery SA | Le Noirmont Jura, Switzerland | Exporter to the US, Foreign private label distributor, Manufacturer, Specification developer | 3 | November 2, 2022 | 0 | 1 | 0 | api.fda.gov |
| Synthes GMBH | Zuchwil Solothurn, Switzerland | Specification developer | 3 | March 27, 2018 | 0 | 0 | 0 | api.fda.gov |
| Abnox AG | Cham Zug, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bruetsch Technology AG | Beringen Schaffhausen, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Frueh Verpackungstechnik AG | Fehraltorf Zurich, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jabil Switzerland Manufacturing GmbH (Bettlach) | Bettlach Solothurn, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nouvag AG | GOLDACH Sankt Gallen, Switzerland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Storz Endoskop Produktions GMBH | Schaffhausen, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SYNTHES GMBH / Synthes Produktions GmbH | Oberdorf, Baselland Basel-Landschaft, Switzerland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.