Data / Medical devices / Orthopedic Stereotaxic Instrument / Switzerland

FDA-registered makers of Orthopedic Stereotaxic Instrument in Switzerland: 21 establishments

Name: FDA-registered makers of Orthopedic Stereotaxic Instrument in Switzerland
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

21 establishments in Switzerland are registered with the FDA to make Orthopedic Stereotaxic Instrument (product code OLO). 9 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: Orthopedic Stereotaxic Instrument
Product code: OLO
Country: Switzerland

Makers of Orthopedic Stereotaxic Instrument in Switzerland

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
Medos International Sarl	Le Locle Neuchatel, Switzerland	Specification developer	16	May 26, 2026	1	api.fda.gov
Spineart SA	Plan-les-Ouates, Switzerland	Complaint file establishment, Specification developer	7	July 29, 2026	0	api.fda.gov
STRYKER GmbH	SELZACH Solothurn, Switzerland	Contract manufacturer, Manufacturer	3	December 18, 2020	0	api.fda.gov
LEM Surgical AG	Bern, Switzerland	Manufacturer	2	June 20, 2026	0	api.fda.gov
Naviswiss AG	Brugg Aargau, Switzerland	Manufacturer	2	January 31, 2023	0	api.fda.gov
Comerge AG	Zurich, Switzerland	Manufacturer	1	March 8, 2024	0	api.fda.gov
Icotec AG	Altstaetten Sankt Gallen, Switzerland	Complaint file establishment, Manufacturer	1	June 27, 2023	0	api.fda.gov
Medacta International SA	Castel San Pietro Ticino, Switzerland	Complaint file establishment, Manufacturer	1	January 15, 2009	0	api.fda.gov
Medacta International SA	Rancate Ticino, Switzerland	Complaint file establishment, Manufacturer	1	January 15, 2009	0	api.fda.gov
Baechler Feintech AG	Hoelstein Basel-Landschaft, Switzerland	Contract manufacturer	0		0	api.fda.gov
Boillat Decolletage SA	Loveresse Bern, Switzerland	Contract manufacturer	0		0	api.fda.gov
Frueh Verpackungstechnik AG	Fehraltorf Zurich, Switzerland	Contract manufacturer	0		0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Balsthal)	Balsthal Solothurn, Switzerland	Contract manufacturer	0		0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Hagendorf)	Hagendorf Solothurn, Switzerland	Contract manufacturer	0		0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Le Locle)	Le Locle Neuchatel, Switzerland	Contract manufacturer	0		0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Raron)	Raron Valais, Switzerland	Contract manufacturer	0		0	api.fda.gov
Leitner AG	Busswil Bern, Switzerland	Contract manufacturer	0		0	api.fda.gov
Moser-Baer AG	Sumiswald Bern, Switzerland	Contract manufacturer	0		0	api.fda.gov
Synthes GMBH	Zuchwil Solothurn, Switzerland	Specification developer	0		0	api.fda.gov
Synthes GMBH	Selzach Solothurn, Switzerland	Manufacturer	0		0	api.fda.gov
Wymed Precision Mechanics	Embrach Zurich, Switzerland	Contract manufacturer	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.