Data / Medical devices / Source, Carrier, Fiberoptic Light / Germany

FDA-registered makers of Source, Carrier, Fiberoptic Light in Germany: 20 establishments

Name: FDA-registered makers of Source, Carrier, Fiberoptic Light in Germany
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

20 establishments in Germany are registered with the FDA to make Source, Carrier, Fiberoptic Light (product code EQH). 1 has 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: Source, Carrier, Fiberoptic Light
Product code: EQH
Country: Germany

Makers of Source, Carrier, Fiberoptic Light in Germany

Maker	Location	Role	510(k) clearances	Latest clearance	Source
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	Manufacturer	1	May 22, 1987	api.fda.gov
Atmos Medizintechnik GMBH & Co. KG	LENZKIRCH Baden-Wurttemberg, Germany	Exporter to the US, Manufacturer	0		api.fda.gov
Dimeda Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Erchinger AG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Evonos GMBH & Co. KG	Tuttlingen Baden-Wurttemberg, Germany	Manufacturer	0		api.fda.gov
Fentexmedical GMBH	NEUHAUSEN, BW Baden-Wurttemberg, Germany	Contract manufacturer, Exporter to the US, Manufacturer	0		api.fda.gov
Hebumedical GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	0		api.fda.gov
Karl Storz Se & Co KG	TUTTLINGEN Baden-Wurttemberg, Germany	Specification developer	0		api.fda.gov
Karl Storz Se & Co. KG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Karl Storz Se & Co. KG	NEUHAUSEN OBECK Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Mattes Instrumente GMBH	Tuttlingen-Nendingen Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	0		api.fda.gov
Med2b Ltd.	Kitzingen Bavaria, Germany	Manufacturer	0		api.fda.gov
Olympus Winter & Ibe GMBH	Hamburg, Germany	Complaint file establishment, Exporter to the US, Specification developer	0		api.fda.gov
Richard Wolf GMBH	KNITTLINGEN Baden-Wurttemberg, Germany	Manufacturer	0		api.fda.gov
Rudolf Riester GMBH	JUNGINGEN Baden-Wurttemberg, Germany	Manufacturer	0		api.fda.gov
RZ Medizintechnik GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Schoelly Fiberoptic, GMBH	DENZLINGEN Baden-Wurttemberg, Germany	Manufacturer	0		api.fda.gov
Symmetry Surgical GmbH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Tekno Medical Optik-Chirurgie GMBH	TUTTLINGEN-Nendingen Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	0		api.fda.gov
Tigris Elektronik GMBH	Berlin, Germany	Contract manufacturer	0		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.