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Data / Medical devices / Broach / Switzerland

FDA-registered makers of Broach in Switzerland: 8 establishments

8 establishments in Switzerland are registered with the FDA to make Broach (product code HTQ). 0 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
Broach
Product code
HTQ
Country
Switzerland

Makers of Broach in Switzerland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Innotool&greminger AGErlen Thurgau, SwitzerlandContract manufacturer0000api.fda.gov
Jabil Switzerland Manufacturing GmbH (Hagendorf)Hagendorf Solothurn, SwitzerlandContract manufacturer0000api.fda.gov
Medos International SarlLe Locle Neuchatel, SwitzerlandSpecification developer0000api.fda.gov
Moser-Baer AGSumiswald Bern, SwitzerlandContract manufacturer0000api.fda.gov
MPS Micro Precision Systems AGBiel-Bienne Bern, SwitzerlandContract manufacturer0000api.fda.gov
STRYKER GmbHSELZACH Solothurn, SwitzerlandSpecification developer0000api.fda.gov
Synthes GMBHZuchwil Solothurn, SwitzerlandSpecification developer0000api.fda.gov
Synthes GMBHSelzach Solothurn, 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.