Data / Medical devices / Curette, Ophthalmic / Germany

FDA-registered makers of Curette, Ophthalmic in Germany: 22 establishments

Name: FDA-registered makers of Curette, Ophthalmic in Germany
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

22 establishments in Germany are registered with the FDA to make Curette, Ophthalmic (product code HNZ). 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: Curette, Ophthalmic
Product code: HNZ
Country: Germany

Makers of Curette, Ophthalmic in Germany

Maker	Location	Role	Source
Addn Solutions GMBH & Co. KG	Wurmlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Asanus Medizintechnik GMBH	NEUHAUSEN OBECK Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler, Specification developer	api.fda.gov
Amann Medical GmbH & Co. KG	Emmingen-Liptingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Bernhard Frey	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Bausch & Lomb Incorporated	Eppelheim Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Carl Teufel GMBH & Co. KG	LIPTINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
CM Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Dimeda Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Fetzer Medical GMBH & Co.kg	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Geuder AG	HEIDELBERG Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Geuder AG	HEIDELBERG Baden-Wurttemberg, Germany	Specification developer	api.fda.gov
Hafner Chirurgische Instrumente	BALGHEIM Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Hebumedical GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer, Manufacturer	api.fda.gov
HGR Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Mattes Instrumente GMBH	Tuttlingen-Nendingen Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	api.fda.gov
Med2b Ltd.	Kitzingen Bavaria, Germany	Manufacturer	api.fda.gov
Medicon, E.G.	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Oertel Medical GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
PMS GmbH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
RZ Medizintechnik GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Tekno Medical Optik-Chirurgie GMBH	TUTTLINGEN-Nendingen Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	api.fda.gov
WILDmedical GmbH	Tuttlingen Baden-Wurttemberg, Germany	Contract 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.