Data / Medical devices / Depressor, Tongue, Non-Surgical / Germany

FDA-registered makers of Depressor, Tongue, Non-Surgical in Germany: 19 establishments

Name: FDA-registered makers of Depressor, Tongue, Non-Surgical in Germany
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

19 establishments in Germany are registered with the FDA to make Depressor, Tongue, Non-Surgical (product code FMA). 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: Depressor, Tongue, Non-Surgical
Product code: FMA
Country: Germany

Makers of Depressor, Tongue, Non-Surgical in Germany

Maker	Location	Role	Source
A. Schweickhardt GMBH & Co. KG	Seitingen-Oberflacht Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	api.fda.gov
A.handte Medizintechnik GMBH & Co. KG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	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
Dimeda Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Dufner Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Heine Optotechnik GMBH & Co. KG.	GILCHING Bavaria, Germany	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
Rudolf Storz GMBH	EMMINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Stork Instrumente GMBH	Emmingen-Liptingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Storz Am Mark GMBH	EMMINGEN-LIPTINGEN Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	api.fda.gov
Symmetry Surgical 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
Ustomed Instrumente GMBH & Co. KG	Tuttlingen Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Willy Storz GMBH	Rietheim-Weilheim 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.