Data / Medical devices / Bougie, Urological / Germany

FDA-registered makers of Bougie, Urological in Germany: 21 establishments

Name: FDA-registered makers of Bougie, Urological in Germany
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

21 establishments in Germany are registered with the FDA to make Bougie, Urological (product code FAX). 1 has 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: Bougie, Urological
Product code: FAX
Country: Germany

Makers of Bougie, Urological in Germany

Maker	Location	Role	510(k) clearances	Latest clearance	Source
Karl Storz Se & Co KG	TUTTLINGEN Baden-Wurttemberg, Germany	Specification developer	1	February 7, 1995	api.fda.gov
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	Manufacturer	0		api.fda.gov
Berger Surgical Medical Products GmbH	Neuhausen ob Eck Baden-Wurttemberg, Germany	Manufacturer	0		api.fda.gov
CM Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Dimeda Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Dufner Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	0		api.fda.gov
Fetzer Medical GMBH & Co.kg	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
HGR Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Karl Storz Se & Co. KG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Karl Storz Se & Co. KG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Karl Storz Se & Co. KG	NEUHAUSEN OBECK Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Med2b Ltd.	Kitzingen Bavaria, Germany	Manufacturer	0		api.fda.gov
Opinstruments GMBH	Rosbach vor der Hoehe Hesse, Germany	Manufacturer	0		api.fda.gov
Reda Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Richard Wolf GMBH	KNITTLINGEN Baden-Wurttemberg, Germany	Manufacturer	0		api.fda.gov
Rudolf Medical GMBH + Co. KG	FRIDINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
RZ Medizintechnik GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	0		api.fda.gov
Symmetry Surgical GmbH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Tontarra Medizintechnik GMBH	WURMLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Teufel & Gerlach GmbH	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Zepf Medical Instruments GMBH	SEITINGEN-OBERFLACHT Baden-Wurttemberg, Germany	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.