Data / Medical devices / Posterior Cervical Screw System / Germany

FDA-registered makers of Posterior Cervical Screw System in Germany: 15 establishments

Name: FDA-registered makers of Posterior Cervical Screw System in Germany
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

15 establishments in Germany are registered with the FDA to make Posterior Cervical Screw System (product code NKG). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device: Posterior Cervical Screw System
Product code: NKG
Country: Germany

Makers of Posterior Cervical Screw System in Germany

Maker	Location	Role	510(k) clearances	Latest clearance	Source
Signus Medizintechnik GMBH	ALZENAU Bavaria, Germany	Complaint file establishment, Exporter to the US, Manufacturer, Specification developer	2	November 18, 2022	api.fda.gov
Silony Medical GMBH	Leinfelden-Echterdingen Baden-Wurttemberg, Germany	Complaint file establishment, Specification developer	2	April 7, 2020	api.fda.gov
Ulrich GMBH & Co. KG	ULM Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	2	December 22, 2016	api.fda.gov
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	Manufacturer	1	July 1, 2022	api.fda.gov
Medtronic Sofamor Danek Deggendorf GMBH	DEGGENDORF Bavaria, Germany	Manufacturer	1	August 21, 2017	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
Erchinger AG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Eurofins Inpac Medizintechnik GMBH	Birkenfeld Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Eurofins Inpac Medizintechnik GMBH	Birkenfeld Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Friedrich Daniels GMBH	SOLINGEN North Rhine-Westphalia, Germany	Contract manufacturer	0		api.fda.gov
JAKUTEC MEDIZINTECHNIK GMBH & Co. KG	LIPTINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Procon Medizintechnik GMBH	Alzenau Bavaria, Germany	Contract manufacturer	0		api.fda.gov
Puracon GMBH	Rosenheim Bavaria, Germany	Contract manufacturer	0		api.fda.gov
W+S Solutions GMBH	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov

Updated November 3, 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.