Data / Medical devices / Neurological Stereotaxic Instrument / Germany

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

Name: FDA-registered makers of Neurological 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 Neurological Stereotaxic Instrument (product code HAW). 8 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.

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Device: Neurological Stereotaxic Instrument
Product code: HAW
Country: Germany

Makers of Neurological Stereotaxic Instrument in Germany

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Class I	Source
Brainlab Se	Munich Bavaria, Germany	Exporter to the US, Manufacturer	17	January 28, 2025	9	2	api.fda.gov
Stryker Leibinger GMBH & Co. KG	FREIBURG Baden-Wurttemberg, Germany	Complaint file establishment, Manufacturer, Specification developer	12	February 16, 2023	1	0	api.fda.gov
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	Complaint file establishment, Manufacturer	4	May 23, 2008	0	0	api.fda.gov
Pajunk GMBH Medizintechnologie	GEISINGEN Baden-Wurttemberg, Germany	Complaint file establishment, Contract manufacturer, Manufacturer	2	February 22, 2023	0	0	api.fda.gov
Eemagine Medical Imaging Solutions GMBH	Berlin, Germany	Manufacturer	1	April 8, 2022	0	0	api.fda.gov
Inomed Medizintechnik GMBH	EMMENDINGEN Baden-Wurttemberg, Germany	Manufacturer	1	May 17, 2001	0	0	api.fda.gov
Karl Storz Se & Co KG	TUTTLINGEN Baden-Wurttemberg, Germany	Specification developer	1	September 27, 2012	0	0	api.fda.gov
Localite GMBH	Bonn North Rhine-Westphalia, Germany	Manufacturer	1	April 17, 2023	0	0	api.fda.gov
3C-Medical Intelligence GmbH	Landsberg am Lech Bavaria, Germany	Contract manufacturer	0		0	0	api.fda.gov
Bemotec GMBH	Sonnenbühl Baden-Wurttemberg, Germany	Contract manufacturer	0		0	0	api.fda.gov
DHF Praezisionsmechanik GMBH	Tuntenhausen Bavaria, Germany	Contract manufacturer	0		0	0	api.fda.gov
Eurofins Inpac Medizintechnik GMBH	Birkenfeld Baden-Wurttemberg, Germany	Contract manufacturer	0		0	0	api.fda.gov
Freyer GMBH & Co. KG	Tuningen Baden-Wurttemberg, Germany	Contract manufacturer	0		0	0	api.fda.gov
Friedrich Daniels GMBH	SOLINGEN North Rhine-Westphalia, Germany	Contract manufacturer	0		0	0	api.fda.gov
Hipp Medical AG	Renquishausen Baden-Wurttemberg, Germany	Contract manufacturer	0		0	0	api.fda.gov
JAKUTEC MEDIZINTECHNIK GMBH & Co. KG	LIPTINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		0	0	api.fda.gov
Josef Frech GMBH & Co. KG	Konigsheim Baden-Wurttemberg, Germany	Contract manufacturer	0		0	0	api.fda.gov
Karl Storz Se & Co. KG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		0	0	api.fda.gov
Karl Storz Se & Co. KG	NEUHAUSEN OBECK Baden-Wurttemberg, Germany	Contract manufacturer	0		0	0	api.fda.gov
KLS Martin SE & Co. KG	Muhlheim/Donau Baden-Wurttemberg, Germany	Contract manufacturer	0		0	0	api.fda.gov
Neuromedex GmbH	Hamburg Schleswig-Holstein, Germany	Contract manufacturer	0		0	0	api.fda.gov
RAUMEDIC - Werk Zwoenitz	Zwoenitz Saxony, Germany	Contract manufacturer	0		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.