Data / Medical devices / Material, Tooth Shade, Resin / Germany
FDA-registered makers of Material, Tooth Shade, Resin in Germany: 22 establishments
22 establishments in Germany are registered with the FDA to make Material, Tooth Shade, Resin (product code EBF). 18 have a 510(k) clearance or PMA approval on file and 1 has 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.
- Device
- Material, Tooth Shade, Resin
- Product code
- EBF
- Country
- Germany
Makers of Material, Tooth Shade, Resin in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Voco GMBH | CUXHAVEN Lower Saxony, Germany | Manufacturer | 36 | April 27, 2026 | 0 | 1 | 0 | api.fda.gov |
| Kulzer GMBH | HANAU Hesse, Germany | Exporter to the US, Specification developer | 12 | March 11, 2026 | 0 | 0 | 0 | api.fda.gov |
| Deltamed GMBH | FRIEDBERG Hesse, Germany | Manufacturer | 10 | December 18, 2024 | 0 | 0 | 0 | api.fda.gov |
| S & C Polymer GMBH | ELMSHORN Schleswig-Holstein, Germany | Contract manufacturer, Manufacturer, Repackager or relabeler | 7 | July 3, 2019 | 0 | 0 | 0 | api.fda.gov |
| indigodental GmbH | Pinneberg Schleswig-Holstein, Germany | Exporter to the US, Manufacturer | 6 | November 17, 2010 | 0 | 0 | 0 | api.fda.gov |
| DMG Chemisch Pharmazeutische Fabrik GMBH | Hamburg, Germany | Manufacturer | 5 | January 31, 2018 | 0 | 0 | 0 | api.fda.gov |
| Kettenbach GMBH & Co KG | ESCHENBURG Hesse, Germany | Manufacturer, Repackager or relabeler | 5 | March 14, 2025 | 0 | 0 | 0 | api.fda.gov |
| DENTSPLY DETREY GmbH | KONSTANZ Baden-Wurttemberg, Germany | Contract manufacturer, Manufacturer | 4 | November 20, 2018 | 0 | 0 | 0 | api.fda.gov |
| Vita Zahnfabrik H. Rauter GMBH & Co. KG. | BAD SACKINGEN Baden-Wurttemberg, Germany | Manufacturer, Repackager or relabeler | 4 | September 23, 2022 | 0 | 0 | 0 | api.fda.gov |
| Bego Bremer Goldschlaegerei Wilh. Herbst GMBH & Co. KG | Bremen, Germany | Manufacturer | 2 | November 9, 2023 | 0 | 0 | 0 | api.fda.gov |
| Bredent GMBH & Co.kg | SENDEN Bavaria, Germany | Manufacturer | 2 | July 21, 2016 | 0 | 0 | 0 | api.fda.gov |
| Kavo Dental GMBH | WARTHAUSEN Baden-Wurttemberg, Germany | Manufacturer, Specification developer | 2 | October 14, 2009 | 0 | 0 | 0 | api.fda.gov |
| Solventum Germany GmbH | SEEFELD Bavaria, Germany | Manufacturer | 2 | January 3, 2000 | 0 | 0 | 0 | api.fda.gov |
| Creamed GMBH & Co. Produktions- Und Handels KG | Marburg Hesse, Germany | Manufacturer | 1 | September 9, 2022 | 0 | 0 | 0 | api.fda.gov |
| Detax GMBH | ETTLINGEN Baden-Wurttemberg, Germany | Manufacturer | 1 | September 23, 2022 | 0 | 0 | 0 | api.fda.gov |
| Merz Dental GMBH | LUETJENBURG Schleswig-Holstein, Germany | Manufacturer | 1 | December 18, 2017 | 0 | 0 | 0 | api.fda.gov |
| MK-dent GmbH | Bargteheide Schleswig-Holstein, Germany | Contract manufacturer, Manufacturer | 1 | October 24, 2002 | 0 | 0 | 0 | api.fda.gov |
| anax dent GmbH | Stuttgart Baden-Wurttemberg, Germany | Manufacturer | 1 | January 26, 2012 | 0 | 0 | 0 | api.fda.gov |
| Identa Dental Material GMBH | CUXHAVEN Lower Saxony, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kulzer GMBH | WEHRHEIM Hesse, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MANI MEDICAL GERMANY GmbH | Rosbach Hesse, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| medmix Deutschland GmbH | Kiel Schleswig-Holstein, Germany | Contract manufacturer | 0 | 0 | 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.