Data / Medical devices / Instrument, Cutting, Orthopedic / Germany

FDA-registered makers of Instrument, Cutting, Orthopedic in Germany: 33 establishments

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

33 establishments in Germany are registered with the FDA to make Instrument, Cutting, Orthopedic (product code HTZ). 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: Instrument, Cutting, Orthopedic
Product code: HTZ
Country: Germany

Makers of Instrument, Cutting, Orthopedic 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
Arthrex GmbH	Munich Bavaria, Germany	Specification developer	api.fda.gov
Christian Diener GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract 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
Erchinger AG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Fetzer Medical GMBH & Co.kg	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Friedrich Daniels GMBH	SOLINGEN North Rhine-Westphalia, Germany	Contract manufacturer	api.fda.gov
G. Hipp & Sohn GMBH	NEUHAUSEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Gebrueder Zepf	DUERBHEIM Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Geomed Medizin-Technik GMBH & Co. KG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Hebumedical GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	api.fda.gov
JAKUTEC MEDIZINTECHNIK GMBH & Co. KG	LIPTINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Jabil Tuttlingen Manufacturing GmbH	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Kapp Surgical GMBH	DUERBHEIM Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Karl Klappenecker GMBH & Co. KG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Koscher & Wuertz GMBH	SPAICHINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Mattes Instrumente GMBH	Tuttlingen-Nendingen Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	api.fda.gov
Max Hauser Suddeutsche Chirurgiemechanik GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Med2b Ltd.	Kitzingen Bavaria, Germany	Manufacturer	api.fda.gov
MEDITEC SOURCE GmbH & Co. KG	Tuttlingen-Nendingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Opinstruments GMBH	Rosbach vor der Hoehe Hesse, Germany	Manufacturer	api.fda.gov
PETER HOEHNLE GmbH & Co. KG	FRITTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Pro-Med Instrumente GMBH	TUTTLINGEN 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
Smi Medical Instruments GMBH & Co.kg	NEUHAUSEN OB ECK Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
SMT Schilling Metalltechnik GMBH	MUHLHEIM Baden-Wurttemberg, Germany	Manufacturer	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	Contract manufacturer, Repackager or relabeler	api.fda.gov
Tontarra Medizintechnik GMBH	WURMLINGEN Baden-Wurttemberg, Germany	Contract 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.