Data / Medical devices / Template / Germany

FDA-registered makers of Template in Germany: 33 establishments

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

33 establishments in Germany are registered with the FDA to make Template (product code HWT). 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: Template
Product code: HWT
Country: Germany

Makers of Template in Germany

Maker	Location	Role	Source
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	Complaint file establishment, Contract manufacturer, Manufacturer	api.fda.gov
Armbruster GMBH	Steinach Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Aristotech Industries GmbH	Berlin, Germany	Contract manufacturer	api.fda.gov
Blache Medical GMBH & Co. KG	Wellendingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Bricon Technology GmbH	WURMLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Christian Diener GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract 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
Gebr. Brasseler GMBH & Co. KG	LEMGO North Rhine-Westphalia, Germany	Contract manufacturer	api.fda.gov
Hermann Medizintechnik GMBH	FRIDINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
HGR Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Heraeus Medical GmbH	WEHRHEIM Hesse, Germany	Manufacturer	api.fda.gov
Hipp Medical AG	Renquishausen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Ilg Medizintechnik GMBH	DURCHHAUSEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Jabil Tuttlingen Manufacturing GmbH	Tuttlingen 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
Medcare Solutions GMBH	Emmingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Medicon, E.G.	TUTTLINGEN Baden-Wurttemberg, Germany	Complaint file establishment, Manufacturer	api.fda.gov
MEDITEC SOURCE GmbH & Co. KG	Tuttlingen-Nendingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Merete GMBH	Berlin, Germany	Specification developer	api.fda.gov
Osartis GMBH	Muenster Hesse, Germany	Specification developer	api.fda.gov
Puracon GMBH	Rosenheim Bavaria, Germany	Contract manufacturer	api.fda.gov
Rudolf Storz GMBH	EMMINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Signus Medizintechnik GMBH	ALZENAU Bavaria, Germany	Complaint file establishment, Exporter to the US, Specification developer	api.fda.gov
Stork Instrumente GMBH	Emmingen-Liptingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Stryker Leibinger GMBH & Co. KG	FREIBURG Baden-Wurttemberg, Germany	Complaint file establishment, Manufacturer	api.fda.gov
Tontarra Medizintechnik GMBH	WURMLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
W+S Solutions GMBH	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Warema Kunststofftechnik Und Maschinenbau GMBH	Marktheidenfeld Bavaria, Germany	Contract manufacturer	api.fda.gov
Waldemar Link GmbH & Co. KG	Norderstedt Schleswig-Holstein, Germany	Manufacturer	api.fda.gov
implantcast GmbH	Buxtehude Lower Saxony, Germany	Complaint file establishment, Exporter to the US, 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.