Data / Medical devices / Camera, Surgical And Accessories / Germany

FDA-registered makers of Camera, Surgical And Accessories in Germany: 19 establishments

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

19 establishments in Germany are registered with the FDA to make Camera, Surgical And Accessories (product code KQM). 0 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: Camera, Surgical And Accessories
Product code: KQM
Country: Germany

Makers of Camera, Surgical And Accessories in Germany

Maker	Location	Role	Source
Adlink Technology GMBH	Deggendorf Bavaria, Germany	Manufacturer	api.fda.gov
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Berchtold GMBH & Co. KG	TUTTLINGEN Baden-Wurttemberg, Germany	Specification developer	api.fda.gov
Baxter Medical Systems GmbH + Co. KG	Munich Bavaria, Germany	Specification developer	api.fda.gov
Baxter Medical Systems GmbH + Co. KG	SAALFELD Thuringia, Germany	Complaint file establishment, Manufacturer	api.fda.gov
Carl Zeiss Meditec AG (oberkochen)	OBERKOCHEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Custom Surgical GMBH	Munich Bavaria, Germany	Manufacturer	api.fda.gov
EIZO GmbH	Ruelzheim Rhineland-Palatinate, Germany	Manufacturer	api.fda.gov
Heinrich Medizintechnik GMBH	Stuttgart Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Heager GmbH	HAAN North Rhine-Westphalia, Germany	Manufacturer, Repackager or relabeler, Specification developer	api.fda.gov
Ilo Electronic GMBH	Kaltenkirchen Schleswig-Holstein, Germany	Manufacturer	api.fda.gov
Joimax GMBH	KARLSRUHE Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
NDS Surgical Imaging, LLC	Ludwigsstadt Bavaria, Germany	Manufacturer	api.fda.gov
Nexor Medical GMBH	Neuhausen ob Eck Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Novanta Medical GmbH	LUDWIGSSTADT Bavaria, Germany	Contract manufacturer	api.fda.gov
Oculus Optikgerate GMBH	WETZLAR Hesse, Germany	Manufacturer	api.fda.gov
Rein Medical GMBH	Moenchengladbach North Rhine-Westphalia, Germany	Manufacturer	api.fda.gov
Richard Wolf GMBH	KNITTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
S.I.M.E.O.N. MEDICAL GMBH & Co.KG	TUTTLINGEN Baden-Wurttemberg, Germany	Complaint file establishment, Contract manufacturer, Manufacturer	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.