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Data / Medical devices / Crown And Bridge, Temporary, Resin / Germany

FDA-registered makers of Crown And Bridge, Temporary, Resin in Germany: 21 establishments

21 establishments in Germany are registered with the FDA to make Crown And Bridge, Temporary, Resin (product code EBG). 19 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.

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Device
Crown And Bridge, Temporary, Resin
Product code
EBG
Country
Germany

Makers of Crown And Bridge, Temporary, Resin in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
DMG Chemisch Pharmazeutische Fabrik GMBHHamburg, GermanyManufacturer4May 29, 2019000api.fda.gov
Voco GMBHCUXHAVEN Lower Saxony, GermanyManufacturer4September 9, 2020000api.fda.gov
Solventum Germany GmbHSEEFELD Bavaria, GermanyManufacturer3January 9, 2008000api.fda.gov
anax dent GmbHStuttgart Baden-Wurttemberg, GermanyManufacturer3December 16, 2010000api.fda.gov
Detax GMBHETTLINGEN Baden-Wurttemberg, GermanyManufacturer2October 27, 2020000api.fda.gov
Merz Dental GMBHLUETJENBURG Schleswig-Holstein, GermanyManufacturer2May 2, 2008000api.fda.gov
S & C Polymer GMBHELMSHORN Schleswig-Holstein, GermanyContract manufacturer, Manufacturer, Repackager or relabeler2February 14, 2001000api.fda.gov
Bego Bremer Goldschlaegerei Wilh. Herbst GMBH & Co. KGBremen, GermanyManufacturer1May 18, 2020000api.fda.gov
Degudent GMBHHANAU Hesse, GermanyManufacturer1December 16, 2010000api.fda.gov
Deltamed GMBHFRIEDBERG Hesse, GermanyManufacturer1July 31, 2020000api.fda.gov
Dreve Dentamid GMBHUNNA North Rhine-Westphalia, GermanyManufacturer1May 31, 2024000api.fda.gov
Kettenbach GMBH & Co KGESCHENBURG Hesse, GermanyManufacturer1December 27, 2012000api.fda.gov
Kulzer GMBHHANAU Hesse, GermanyExporter to the US, Manufacturer1May 23, 2024000api.fda.gov
Pro3dure Medical GMBHIserlohn North Rhine-Westphalia, GermanyManufacturer1November 5, 2020000api.fda.gov
Schuetz Dental GMBHROSBACH Hesse, GermanyManufacturer1February 12, 2015000api.fda.gov
Solventum Germany GmbHKamen North Rhine-Westphalia, GermanyComplaint file establishment, Specification developer1January 9, 2008000api.fda.gov
Vita Zahnfabrik H. Rauter GMBH & Co. KG.BAD SACKINGEN Baden-Wurttemberg, GermanyManufacturer, Repackager or relabeler1June 1, 2007000api.fda.gov
Whitepeaks Dental Solutions GMBHHamminkeln North Rhine-Westphalia, GermanyManufacturer1December 18, 2013000api.fda.gov
etkon GMBHMarkkleeberg Saxony, GermanyManufacturer1August 21, 2007000api.fda.gov
Identa Dental Material GMBHCUXHAVEN Lower Saxony, GermanyContract manufacturer0000api.fda.gov
Kulzer GMBHWEHRHEIM Hesse, GermanyContract manufacturer0000api.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.