Data / Medical devices / Bur, Dental / Germany

FDA-registered makers of Bur, Dental in Germany: 23 establishments

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

23 establishments in Germany are registered with the FDA to make Bur, Dental (product code EJL). 1 has a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device: Bur, Dental
Product code: EJL
Country: Germany

Makers of Bur, Dental in Germany

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
Gebr. Brasseler GMBH & Co. KG	LEMGO North Rhine-Westphalia, Germany	Contract manufacturer, Manufacturer	1	June 29, 2007	0	api.fda.gov
ACURATA GMBH & CO. KGaA	Thurmansbang Bavaria, Germany	Manufacturer	0		0	api.fda.gov
Altatec GMBH	WIMSHEIM Baden-Wurttemberg, Germany	Manufacturer	0		0	api.fda.gov
BUSCH & CO. GmbH & Co. KG	ENGELSKIRCHEN North Rhine-Westphalia, Germany	Contract manufacturer, Manufacturer	0		0	api.fda.gov
Devemed GMBH	NEUHAUSEN OB ECK Baden-Wurttemberg, Germany	Contract manufacturer	0		0	api.fda.gov
Dfs-Diamon GMBH	RIEDENBURG Bavaria, Germany	Manufacturer	0		0	api.fda.gov
DMG Chemisch Pharmazeutische Fabrik GMBH	Hamburg, Germany	Manufacturer	0		0	api.fda.gov
DR. Hopf GMBH & Co. KG	LANGENHAGEN Lower Saxony, Germany	Manufacturer	0		0	api.fda.gov
Dentaurum GmbH & Co. KG	ISPRINGEN Baden-Wurttemberg, Germany	Manufacturer	0		0	api.fda.gov
Hager & Meisinger GMBH	NEUSS North Rhine-Westphalia, Germany	Contract manufacturer, Manufacturer	0		2	api.fda.gov
Hager & Werken GMBH	DUISBURG,DE-NOTA Hamburg, Germany	Manufacturer	0		0	api.fda.gov
Helmut Zepf Medizintechnik GMBH	SEITINGEN Baden-Wurttemberg, Germany	Exporter to the US, Manufacturer	0		0	api.fda.gov
Hopf, Ringleb & Co. GMBH & Cie.	Berlin, Germany	Manufacturer	0		0	api.fda.gov
Hufschmied Zerspanungssysteme GMBH	Bobingen Bavaria, Germany	Contract manufacturer	0		0	api.fda.gov
Nti-Kahla GMBH, Rotary Dental Instruments	KAHLA Thuringia, Germany	Manufacturer, Repackager or relabeler	0		0	api.fda.gov
Ot Medical GMBH	Bremen, Germany	Manufacturer	0		0	api.fda.gov
Otto Leibinger GMBH	MUEHLHEIM Baden-Wurttemberg, Germany	Contract manufacturer	0		0	api.fda.gov
PSM Medical GmbH	Gunningen Baden-Wurttemberg, Germany	Manufacturer	0		0	api.fda.gov
Puracon GMBH	Rosenheim Bavaria, Germany	Contract manufacturer	0		0	api.fda.gov
Sicat GMBH & Co. KG	BONN North Rhine-Westphalia, Germany	Manufacturer	0		0	api.fda.gov
Storz Am Mark GMBH	EMMINGEN-LIPTINGEN Baden-Wurttemberg, Germany	Manufacturer	0		0	api.fda.gov
Solventum Germany GmbH	SEEFELD Bavaria, Germany	Manufacturer, Repackager or relabeler	0		0	api.fda.gov
Ustomed Instrumente GMBH & Co. KG	Tuttlingen Baden-Wurttemberg, Germany	Manufacturer	0		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.