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Data / Medical devices / Motor, Surgical Instrument, Ac-Powered / Switzerland

FDA-registered makers of Motor, Surgical Instrument, Ac-Powered in Switzerland: 7 establishments

7 establishments in Switzerland are registered with the FDA to make Motor, Surgical Instrument, Ac-Powered (product code GEY). 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
Motor, Surgical Instrument, Ac-Powered
Product code
GEY
Country
Switzerland

Makers of Motor, Surgical Instrument, Ac-Powered in Switzerland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Synthes GMBHZuchwil Solothurn, SwitzerlandSpecification developer1May 5, 1997000api.fda.gov
Baechler Feintech AGHoelstein Basel-Landschaft, SwitzerlandContract manufacturer0000api.fda.gov
Bien-Air Dental SABiel/Bienne Bern, SwitzerlandManufacturer0000api.fda.gov
Maillefer Instruments Holding SarlBALLAIGUES Vaud, SwitzerlandContract manufacturer0000api.fda.gov
Nouvag AGGOLDACH Sankt Gallen, SwitzerlandManufacturer0000api.fda.gov
SYNTHES GMBH / Synthes Produktions GmbHOberdorf, Baselland Basel-Landschaft, SwitzerlandManufacturer0000api.fda.gov
Zimmer Surgical SA1228 Plan Les Ouates Geneve, SwitzerlandManufacturer0000api.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.