Data / Medical devices / Bender / Germany

FDA-registered makers of Bender in Germany: 30 establishments

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

30 establishments in Germany are registered with the FDA to make Bender (product code HXW). 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: Bender
Product code: HXW
Country: Germany

Makers of Bender 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
Asanus Medizintechnik GMBH	NEUHAUSEN OBECK Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler, Specification developer	api.fda.gov
Blache Medical GMBH & Co. KG	Wellendingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
CM Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Erchinger AG	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
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
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
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
Kreidler Medizintechnik GmbH	Wurmlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Maxxos-Medical GMBH	Mahlstetten Baden-Wurttemberg, Germany	Complaint file establishment, Specification developer	api.fda.gov
Med2b Ltd.	Kitzingen Bavaria, Germany	Manufacturer	api.fda.gov
Medcare Solutions GMBH	Emmingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Medicon, E.G.	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	api.fda.gov
MEDITEC SOURCE GmbH & Co. KG	Tuttlingen-Nendingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Pro-Med Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	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
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
Tontarra Medizintechnik GMBH	WURMLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Wenzler Medizintechnik GmbH	Frittlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
e.l. zepf GmbH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract 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.