Data / Medical devices / Unit, Electrosurgical, Endoscopic (With Or Without Accessories) / Germany

FDA-registered makers of Unit, Electrosurgical, Endoscopic (With Or Without Accessories) in Germany: 15 establishments

Name: FDA-registered makers of Unit, Electrosurgical, Endoscopic (With Or Without Accessories) in Germany
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

15 establishments in Germany are registered with the FDA to make Unit, Electrosurgical, Endoscopic (With Or Without Accessories) (product code KNS). 2 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: Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
Product code: KNS
Country: Germany

Makers of Unit, Electrosurgical, Endoscopic (With Or Without Accessories) in Germany

Maker	Location	Role	510(k) clearances	Latest clearance	Source
Olympus Winter & Ibe GMBH	Hamburg, Germany	Complaint file establishment, Exporter to the US, Manufacturer, Specification developer	2	March 24, 2003	api.fda.gov
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	Manufacturer	1	November 9, 1994	api.fda.gov
Dimeda Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Eurofins STERIPAC GMBH	Calw-Altburg Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Guenter Bissinger Medizintechnik GMBH	TENINGEN Baden-Wurttemberg, Germany	Contract manufacturer, 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	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
Koscher & Wuertz GMBH	SPAICHINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Ovesco Endoscopy AG	Tuebingen Baden-Wurttemberg, Germany	Complaint file establishment, Manufacturer	0		api.fda.gov
Olympus Winter & Ibe GmbH	TELTOW Brandenburg, Germany	Manufacturer	0		api.fda.gov
Richard Wolf GMBH	KNITTLINGEN Baden-Wurttemberg, Germany	Manufacturer	0		api.fda.gov
RZ Medizintechnik GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Tontarra Medizintechnik GMBH	WURMLINGEN 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.