Data / Medical devices / Knife, Ent / Germany

FDA-registered makers of Knife, Ent in Germany: 26 establishments

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

26 establishments in Germany are registered with the FDA to make Knife, Ent (product code KTG). 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: Knife, Ent
Product code: KTG
Country: Germany

Makers of Knife, Ent in Germany

Maker	Location	Role	Source
Ackermann Instrumente GMBH	RIETHEIM, WEILHEIM Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Asanus Medizintechnik GMBH	NEUHAUSEN OBECK Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler, Specification developer	api.fda.gov
CM Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Dimeda Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Evonos GMBH & Co. KG	Tuttlingen Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Fetzer Medical GMBH & Co.kg	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Hafner Chirurgische Instrumente	BALGHEIM Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Hebumedical GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Heinrich Medizintechnik GMBH	Stuttgart Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
HGR Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Instrumed GmbH dba Avalign German Specialty Instruments	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Karl Storz Se & Co KG	TUTTLINGEN Baden-Wurttemberg, Germany	Specification developer	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
Nopa Instruments, Medizintechnik GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
PMS 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
Schmid Medizintechnik GMBH	WURMLINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	api.fda.gov
SIMMANK GmbH & Co.KG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Spiggle & Theis Medizintechnik GMBH	OVERATH North Rhine-Westphalia, Germany	Manufacturer, Repackager or relabeler	api.fda.gov
SUBAN Instruments Germany GmbH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Seid Medical GmbH	DENKINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
e.l. zepf GmbH	TUTTLINGEN 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.