Data / Medical devices / Bit, Drill / Switzerland

FDA-registered makers of Bit, Drill in Switzerland: 22 establishments

Name: FDA-registered makers of Bit, Drill in Switzerland
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

22 establishments in Switzerland are registered with the FDA to make Bit, Drill (product code HTW). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device: Bit, Drill
Product code: HTW
Country: Switzerland

Makers of Bit, Drill in Switzerland

Maker	Location	Role	Recall events	Source
Baechler Feintech AG	Hoelstein Basel-Landschaft, Switzerland	Contract manufacturer	0	api.fda.gov
Bonebridge AG	Zug, Switzerland	Complaint file establishment, Specification developer	0	api.fda.gov
Frueh Verpackungstechnik AG	Fehraltorf Zurich, Switzerland	Contract manufacturer	0	api.fda.gov
Innotool&greminger AG	Erlen Thurgau, Switzerland	Contract manufacturer	0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Balsthal)	Balsthal Solothurn, Switzerland	Contract manufacturer	0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Bettlach)	Bettlach Solothurn, Switzerland	Contract manufacturer	0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Hagendorf)	Hagendorf Solothurn, Switzerland	Contract manufacturer	0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Le Locle)	Le Locle Neuchatel, Switzerland	Contract manufacturer	0	api.fda.gov
Leitner AG	Busswil Bern, Switzerland	Contract manufacturer	0	api.fda.gov
Maillefer Instruments Holding Sarl	BALLAIGUES Vaud, Switzerland	Contract manufacturer	0	api.fda.gov
Medartis AG	BASEL Basel-Stadt, Switzerland	Manufacturer	0	api.fda.gov
Medos International Sarl	Le Locle Neuchatel, Switzerland	Specification developer	0	api.fda.gov
Moser-Baer AG	Sumiswald Bern, Switzerland	Contract manufacturer	0	api.fda.gov
MPS Micro Precision Systems AG	Biel-Bienne Bern, Switzerland	Contract manufacturer, Manufacturer	0	api.fda.gov
Sphinx Tools Ltd	Derendingen Solothurn, Switzerland	Contract manufacturer	0	api.fda.gov
Spineart SA	Plan-les-Ouates, Switzerland	Complaint file establishment, Specification developer	0	api.fda.gov
SQ Products AG	Inwil Luzern, Switzerland	Contract manufacturer	0	api.fda.gov
STRYKER GmbH	SELZACH Solothurn, Switzerland	Contract manufacturer	0	api.fda.gov
Synthes GMBH	Zuchwil Solothurn, Switzerland	Specification developer	0	api.fda.gov
SYNTHES GMBH / Synthes Produktions GmbH	Oberdorf, Baselland Basel-Landschaft, Switzerland	Specification developer	0	api.fda.gov
Synthes GMBH	Selzach Solothurn, Switzerland	Manufacturer	0	api.fda.gov
Zimmer GMBH	WINTERTHUR Zurich, Switzerland	Manufacturer	1	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.