Data / Medical devices / Speculum, Vaginal, Metal / Germany

FDA-registered makers of Speculum, Vaginal, Metal in Germany: 33 establishments

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

33 establishments in Germany are registered with the FDA to make Speculum, Vaginal, Metal (product code HDF). 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: Speculum, Vaginal, Metal
Product code: HDF
Country: Germany

Makers of Speculum, Vaginal, Metal in Germany

Maker	Location	Role	Source
Ackermann Instrumente GMBH	RIETHEIM, WEILHEIM Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	api.fda.gov
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
Bauer Und Haselbarth-Chirurg GMBH	ELLERAU Schleswig-Holstein, Germany	Contract manufacturer, Manufacturer	api.fda.gov
Berger Surgical Medical Products GmbH	Neuhausen ob Eck Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
CM Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Dewimed Medizintechnik GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	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
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
Helmut Zepf Medizintechnik GMBH	SEITINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Hermann Medizintechnik GMBH	FRIDINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
HERMANN MUELLER Medizintechnik 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
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
Med2b Ltd.	Kitzingen Bavaria, Germany	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
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 Riester GMBH	JUNGINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
RZ Medizintechnik GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	api.fda.gov
Stork Instrumente GMBH	Emmingen-Liptingen Baden-Wurttemberg, Germany	Contract 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	Manufacturer, Repackager or relabeler	api.fda.gov
WILDmedical GmbH	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Zepf Medical Instruments GMBH	SEITINGEN-OBERFLACHT Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
medi-plus Instrumente GmbH	TUTTLINGEN-NENDINGEN 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.