Data / Medical devices / Appliance, Fixation, Spinal Intervertebral Body / Germany

FDA-registered makers of Appliance, Fixation, Spinal Intervertebral Body in Germany: 18 establishments

Name: FDA-registered makers of Appliance, Fixation, Spinal Intervertebral Body in Germany
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

18 establishments in Germany are registered with the FDA to make Appliance, Fixation, Spinal Intervertebral Body (product code KWQ). 5 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: Appliance, Fixation, Spinal Intervertebral Body
Product code: KWQ
Country: Germany

Makers of Appliance, Fixation, Spinal Intervertebral Body in Germany

Maker	Location	Role	510(k) clearances	Latest clearance	Source
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	Complaint file establishment, Manufacturer	11	September 11, 2012	api.fda.gov
Signus Medizintechnik GMBH	ALZENAU Bavaria, Germany	Complaint file establishment, Exporter to the US, Manufacturer, Specification developer	3	December 23, 2013	api.fda.gov
Medtronic Sofamor Danek Deggendorf GMBH	DEGGENDORF Bavaria, Germany	Manufacturer	1	July 9, 2014	api.fda.gov
Silony Medical GMBH	Leinfelden-Echterdingen Baden-Wurttemberg, Germany	Complaint file establishment, Specification developer	1	June 8, 2017	api.fda.gov
Ulrich GMBH & Co. KG	ULM Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	1	May 21, 2010	api.fda.gov
Armbruster GMBH	Steinach Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Christian Diener GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Eurofins STERIPAC GMBH	Calw-Altburg Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Friedrich Daniels GMBH	SOLINGEN North Rhine-Westphalia, Germany	Contract manufacturer	0		api.fda.gov
Gebr. Brasseler GMBH & Co. KG	LEMGO North Rhine-Westphalia, Germany	Contract manufacturer	0		api.fda.gov
HG Medical GmbH	Raisting Bavaria, Germany	Contract manufacturer	0		api.fda.gov
Hipp Medical AG	Renquishausen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
JAKUTEC MEDIZINTECHNIK GMBH & Co. KG	LIPTINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Jabil Tuttlingen Manufacturing GmbH	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Medcare Solutions GMBH	Emmingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Procon Medizintechnik GMBH	Alzenau Bavaria, Germany	Contract manufacturer	0		api.fda.gov
Ptumedical GMBH	Spaichingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Puracon GMBH	Rosenheim Bavaria, Germany	Contract manufacturer	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.