Data / Medical devices / Nasopharyngoscope (Flexible Or Rigid) / Germany

FDA-registered makers of Nasopharyngoscope (Flexible Or Rigid) in Germany: 20 establishments

Name: FDA-registered makers of Nasopharyngoscope (Flexible Or Rigid) in Germany
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

20 establishments in Germany are registered with the FDA to make Nasopharyngoscope (Flexible Or Rigid) (product code EOB). 7 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: Nasopharyngoscope (Flexible Or Rigid)
Product code: EOB
Country: Germany

Makers of Nasopharyngoscope (Flexible Or Rigid) in Germany

Maker	Location	Role	510(k) clearances	Latest clearance	Source
Karl Storz Se & Co KG	TUTTLINGEN Baden-Wurttemberg, Germany	Specification developer	28	August 11, 2020	api.fda.gov
Olympus Winter & Ibe GMBH	Hamburg, Germany	Exporter to the US, Manufacturer	3	April 5, 2016	api.fda.gov
Schoelly Fiberoptic, GMBH	DENZLINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	3	March 4, 2015	api.fda.gov
Atmos Medizintechnik GMBH & Co. KG	LENZKIRCH Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	2	August 3, 2023	api.fda.gov
Henke-Sass Wolf, GMBH.	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	2	April 1, 2003	api.fda.gov
Richard Wolf GMBH	KNITTLINGEN Baden-Wurttemberg, Germany	Manufacturer	2	September 24, 1999	api.fda.gov
asap endoscopic products GmbH	Umkirch Baden-Wurttemberg, Germany	Manufacturer	1	January 8, 2004	api.fda.gov
Almikro GMBH & Co. KG	Bad Krozingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Bowa-Electronic GMBH	GOMARINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Faulhaber Pinzetten KG	FRITTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
HGR Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
JR Montagearbeiten	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Jr-Medizintechnik GMBH & Co KG	Leibertingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Karl Storz Se & Co. KG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	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
Kunststoff Helmbrechts AG	Helmbrechts Bavaria, Germany	Contract manufacturer	0		api.fda.gov
Sutter Medizintechnik GMBH	Emmendingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Teufel & Gerlach GmbH	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
medi-G GMBH	Messkirch Baden-Wurttemberg, 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.