Data / Medical devices / Laparoscope, Gynecologic (And Accessories) / Germany

FDA-registered makers of Laparoscope, Gynecologic (And Accessories) in Germany: 32 establishments

Name: FDA-registered makers of Laparoscope, Gynecologic (And Accessories) in Germany
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

32 establishments in Germany are registered with the FDA to make Laparoscope, Gynecologic (And Accessories) (product code HET). 13 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: Laparoscope, Gynecologic (And Accessories)
Product code: HET
Country: Germany

Makers of Laparoscope, Gynecologic (And Accessories) in Germany

Maker	Location	Role	510(k) clearances	Latest clearance	Source
Karl Storz Se & Co KG	TUTTLINGEN Baden-Wurttemberg, Germany	Specification developer	15	November 20, 2015	api.fda.gov
Richard Wolf GMBH	KNITTLINGEN Baden-Wurttemberg, Germany	Manufacturer	9	June 29, 2009	api.fda.gov
Gimmi GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	2	March 11, 2004	api.fda.gov
Guenter Bissinger Medizintechnik GMBH	TENINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	2	March 11, 2004	api.fda.gov
Novanta Medical GmbH	LUDWIGSSTADT Bavaria, Germany	Manufacturer	2	March 21, 2017	api.fda.gov
Novanta Medical GmbH	Berlin, Germany	Specification developer	2	March 21, 2017	api.fda.gov
Olympus Winter & Ibe GMBH	Hamburg, Germany	Complaint file establishment, Exporter to the US, Manufacturer, Specification developer	2	August 29, 2019	api.fda.gov
Innoview GMBH	Eichstetten Baden-Wurttemberg, Germany	Manufacturer	1	February 18, 1999	api.fda.gov
Med Contact GMBH	Burladingen-Salmendingen Baden-Wurttemberg, Germany	Specification developer	1	September 15, 1995	api.fda.gov
Olympus Winter & Ibe GmbH	TELTOW Brandenburg, Germany	Manufacturer	1	February 22, 1996	api.fda.gov
Pajunk GMBH Medizintechnologie	GEISINGEN Baden-Wurttemberg, Germany	Manufacturer	1	October 13, 2006	api.fda.gov
Schoelly Fiberoptic, GMBH	DENZLINGEN Baden-Wurttemberg, Germany	Manufacturer	1	March 12, 2021	api.fda.gov
Trokamed GMBH	GEISINGEN Baden-Wurttemberg, Germany	Manufacturer	1	March 1, 2011	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
Bowa-Electronic GMBH	GOMARINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Boyd Weiler GmbH & Co. KG	Weiler-Simmerberg Bavaria, Germany	Contract manufacturer	0		api.fda.gov
Dufner Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	0		api.fda.gov
Eurofins STERIPAC GMBH	Calw-Altburg Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Henke-Sass Wolf, GMBH.	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
HGR Instrumente GMBH	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
Koscher & Wuertz GMBH	SPAICHINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Medcare Solutions GMBH	Emmingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Rudolf Medical GMBH + Co. KG	FRIDINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
RZ Medizintechnik GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Strub Medical GmbH & Co. KG	NEUHAUSEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Tontarra Medizintechnik GMBH	WURMLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
asap endoscopic products GmbH	Umkirch Baden-Wurttemberg, Germany	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.