Data / Medical devices / Mirror, Ent / Germany

FDA-registered makers of Mirror, Ent in Germany: 28 establishments

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

28 establishments in Germany are registered with the FDA to make Mirror, Ent (product code KAI). 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: Mirror, Ent
Product code: KAI
Country: Germany

Makers of Mirror, Ent in Germany

Maker	Location	Role	Source
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Berger Surgical Medical Products GmbH	Neuhausen ob Eck Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Dufner Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
E. Hahnenkratt GMBH	KOENIGSBACH-STEIN Baden-Wurttemberg, Germany	Contract manufacturer, 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
Hebumedical GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer, 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	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
Mattes Instrumente GMBH	Tuttlingen-Nendingen Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	api.fda.gov
Medcare Solutions GMBH	Emmingen Baden-Wurttemberg, Germany	Contract 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
Pfau Medizinische Instrumente GMBH	WANFRIED Hesse, Germany	Contract manufacturer	api.fda.gov
PMS GmbH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract 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	api.fda.gov
Strub Medical GmbH & Co. KG	NEUHAUSEN 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
WILDmedical GmbH	Tuttlingen 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.