Data / Medical devices / Orthopedic Stereotaxic Instrument / Germany

FDA-registered makers of Orthopedic Stereotaxic Instrument in Germany: 22 establishments

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

22 establishments in Germany are registered with the FDA to make Orthopedic Stereotaxic Instrument (product code OLO). 6 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: Germany

Makers of Orthopedic Stereotaxic Instrument in Germany

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
Stryker Leibinger GMBH & Co. KG	FREIBURG Baden-Wurttemberg, Germany	Complaint file establishment, Contract manufacturer, Manufacturer, Specification developer	18	February 19, 2026	0	api.fda.gov
Brainlab Se	Munich Bavaria, Germany	Manufacturer	11	September 30, 2026	5	api.fda.gov
Silony Medical GMBH	Leinfelden-Echterdingen Baden-Wurttemberg, Germany	Manufacturer, Specification developer	4	June 26, 2026	0	api.fda.gov
Fiagon GMBH	Hennigsdorf Brandenburg, Germany	Manufacturer	1	November 20, 2023	0	api.fda.gov
Joimax GMBH	KARLSRUHE Baden-Wurttemberg, Germany	Exporter to the US, Manufacturer	1	July 30, 2020	0	api.fda.gov
Medtronic Sofamor Danek Deggendorf GMBH	DEGGENDORF Bavaria, Germany	Manufacturer	1	February 12, 2026	0	api.fda.gov
Armbruster GMBH	Steinach Baden-Wurttemberg, Germany	Contract manufacturer	0		0	api.fda.gov
Christian Diener GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		0	api.fda.gov
DHF Praezisionsmechanik GMBH	Tuntenhausen Bavaria, Germany	Contract manufacturer	0		0	api.fda.gov
Erchinger AG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		0	api.fda.gov
Eurofins Inpac Medizintechnik GMBH	Birkenfeld Baden-Wurttemberg, Germany	Contract manufacturer	0		0	api.fda.gov
Friedrich Daniels GMBH	SOLINGEN North Rhine-Westphalia, Germany	Contract manufacturer	0		0	api.fda.gov
Gebr. Brasseler GMBH & Co. KG	LEMGO North Rhine-Westphalia, Germany	Contract manufacturer	0		0	api.fda.gov
Hebumedical GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		0	api.fda.gov
Hipp Medical AG	Renquishausen Baden-Wurttemberg, Germany	Contract manufacturer	0		0	api.fda.gov
JAKUTEC MEDIZINTECHNIK GMBH & Co. KG	LIPTINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		0	api.fda.gov
Kammerer Medical Systems GmbH & Co. KG	Stockach Baden-Wurttemberg, Germany	Contract manufacturer	0		0	api.fda.gov
Quintenz Hybridtechnik GMBH	Neuried Bavaria, Germany	Contract manufacturer	0		0	api.fda.gov
Stryker Trauma GMBH	SCHOENKIRCHEN Schleswig-Holstein, Germany	Contract manufacturer	0		0	api.fda.gov
Tontarra Medizintechnik GMBH	WURMLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		0	api.fda.gov
Ulrich GMBH & Co. KG	ULM Baden-Wurttemberg, Germany	Contract manufacturer	0		0	api.fda.gov
W+S Solutions GMBH	Tuttlingen Baden-Wurttemberg, Germany	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.