Data / Medical devices / Gag, Mouth / Germany

FDA-registered makers of Gag, Mouth in Germany: 34 establishments

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

34 establishments in Germany are registered with the FDA to make Gag, Mouth (product code KBN). 0 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: Gag, Mouth
Product code: KBN
Country: Germany

Makers of Gag, Mouth in Germany

Maker	Location	Role	Source
A. Schweickhardt GMBH & Co. KG	Seitingen-Oberflacht Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	api.fda.gov
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
CM Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Devemed GMBH	NEUHAUSEN OB ECK Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	api.fda.gov
Dimeda Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Dufner Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Fetzer Medical GMBH & Co.kg	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Hebumedical GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	api.fda.gov
Helmut Zepf Medizintechnik GMBH	SEITINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
HERMANN MUELLER Medizintechnik GmbH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	api.fda.gov
JOSEF BETZLER SURGICAL INSTRUMENTS e.K.	SEITINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Karl Hammacher GMBH	SOLINGEN North Rhine-Westphalia, Germany	Manufacturer	api.fda.gov
Karl Storz Se & Co KG	TUTTLINGEN Baden-Wurttemberg, Germany	Specification developer	api.fda.gov
Karl Storz Se & Co. KG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Karl Storz Se & Co. KG	NEUHAUSEN OBECK Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
KLS Martin Se & Co. KG	Fridingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
KLS Martin SE & Co. KG	Muhlheim/Donau Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Kohler Medizintechnik GmbH	STOCKACH Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	api.fda.gov
Kreidler Medizintechnik GmbH	Wurmlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Med2b Ltd.	Kitzingen Bavaria, Germany	Manufacturer	api.fda.gov
Medical Bees GMBH	Emmingen-Liptingen Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Medicon, E.G.	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Nopa Instruments, Medizintechnik GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Reda Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Richard Wolf GMBH	KNITTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Rudolf Medical GMBH + Co. KG	FRIDINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Rudolf Storz GMBH	EMMINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
RZ Medizintechnik GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	api.fda.gov
Storz Am Mark GMBH	EMMINGEN-LIPTINGEN Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	api.fda.gov
SUBAN Instruments Germany GmbH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Tekno Medical Optik-Chirurgie GMBH	TUTTLINGEN-Nendingen Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	api.fda.gov
Teufel & Gerlach GmbH	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Ustomed Instrumente GMBH & Co. KG	Tuttlingen Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Zepf Medical Instruments GMBH	SEITINGEN-OBERFLACHT Baden-Wurttemberg, Germany	Manufacturer	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.