Data / Medical devices / Ureteroscope And Accessories, Flexible/Rigid / Germany

FDA-registered makers of Ureteroscope And Accessories, Flexible/Rigid in Germany: 17 establishments

Name: FDA-registered makers of Ureteroscope And Accessories, Flexible/Rigid in Germany
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

17 establishments in Germany are registered with the FDA to make Ureteroscope And Accessories, Flexible/Rigid (product code FGB). 6 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers of this device in Germany Watch these makers

Device: Ureteroscope And Accessories, Flexible/Rigid
Product code: FGB
Country: Germany

Makers of Ureteroscope And Accessories, Flexible/Rigid in Germany

Maker	Location	Role	510(k) clearances	Latest clearance	Source
Karl Storz Se & Co KG	TUTTLINGEN Baden-Wurttemberg, Germany	Specification developer	14	November 18, 2025	api.fda.gov
Richard Wolf GMBH	KNITTLINGEN Baden-Wurttemberg, Germany	Manufacturer	4	January 15, 2021	api.fda.gov
Olympus Winter & Ibe GMBH	Hamburg, Germany	Complaint file establishment, Exporter to the US, Manufacturer, Specification developer	3	August 28, 2020	api.fda.gov
Henke-Sass Wolf, GMBH.	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Exporter to the US	1	September 12, 2012	api.fda.gov
Innoview GMBH	Eichstetten Baden-Wurttemberg, Germany	Manufacturer	1	December 8, 2006	api.fda.gov
Schoelly Fiberoptic, GMBH	DENZLINGEN Baden-Wurttemberg, Germany	Manufacturer	1	October 13, 1999	api.fda.gov
Almikro GMBH & Co. KG	Bad Krozingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Bacher Medizintechnik GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Boyd Weiler GmbH & Co. KG	Weiler-Simmerberg Bavaria, Germany	Contract manufacturer	0		api.fda.gov
Haager GMBH & Co. KG	Pforzheim 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
OSYPKA GmbH	Rheinfelden Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Pajunk GMBH Medizintechnologie	GEISINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Rudolf Medical GMBH + Co. KG	FRIDINGEN 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.