FDA-registered makers of Awl in Germany: 36 establishments

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

36 establishments in Germany are registered with the FDA to make Awl (product code HWJ). 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: Awl
Product code: HWJ
Country: Germany

Makers of Awl in Germany

Maker	Location	Role	Source
Addn Solutions GMBH & Co. KG	Wurmlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Armbruster GMBH	Steinach Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Asanus Medizintechnik GMBH	NEUHAUSEN OBECK Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler, Specification developer	api.fda.gov
Aristotech Industries GmbH	Berlin, Germany	Contract manufacturer	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
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
Hafner Chirurgische Instrumente	BALGHEIM Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Helmut Zepf Medizintechnik GMBH	SEITINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	api.fda.gov
Joimax GMBH	KARLSRUHE Baden-Wurttemberg, Germany	Exporter to the US, 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
Kammerer Medical Systems GmbH & Co. KG	Stockach Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Med2b Ltd.	Kitzingen Bavaria, Germany	Manufacturer	api.fda.gov
Medicon, E.G.	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Merete GMBH	Berlin, Germany	Specification developer	api.fda.gov
Opinstruments GMBH	Rosbach vor der Hoehe Hesse, Germany	Manufacturer	api.fda.gov
PMS GmbH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Reda Instrumente 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
Silony Medical GMBH	Leinfelden-Echterdingen Baden-Wurttemberg, Germany	Manufacturer, Specification developer	api.fda.gov
Stork Instrumente GMBH	Emmingen-Liptingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Stryker Trauma GMBH	SCHOENKIRCHEN Schleswig-Holstein, Germany	Contract manufacturer	api.fda.gov
Stengelin Medical GmbH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Teufel & Gerlach GmbH	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Ulrich GMBH & Co. KG	ULM Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Ustomed Instrumente GMBH & Co. KG	Tuttlingen Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Waldemar Link GmbH & Co. KG	Norderstedt Schleswig-Holstein, Germany	Manufacturer	api.fda.gov
Zepf Medical Instruments GMBH	SEITINGEN-OBERFLACHT Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
implantcast GmbH	Buxtehude Lower Saxony, Germany	Complaint file establishment, Exporter to the US, Manufacturer	api.fda.gov
medi-plus Instrumente GmbH	TUTTLINGEN-NENDINGEN 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.