Data / Medical devices / Cement, Dental / Germany
FDA-registered makers of Cement, Dental in Germany: 12 establishments
12 establishments in Germany are registered with the FDA to make Cement, Dental (product code EMA). 10 have 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
- Cement, Dental
- Product code
- EMA
- Country
- Germany
Makers of Cement, Dental in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Solventum Germany GmbH | SEEFELD Bavaria, Germany | Manufacturer | 16 | November 5, 2019 | 0 | 0 | 0 | api.fda.gov |
| Voco GMBH | CUXHAVEN Lower Saxony, Germany | Manufacturer | 15 | March 20, 2026 | 0 | 1 | 0 | api.fda.gov |
| DMG Chemisch Pharmazeutische Fabrik GMBH | Hamburg, Germany | Manufacturer | 7 | June 1, 2022 | 0 | 0 | 0 | api.fda.gov |
| S & C Polymer GMBH | ELMSHORN Schleswig-Holstein, Germany | Contract manufacturer, Manufacturer, Repackager or relabeler | 6 | September 25, 2009 | 0 | 0 | 0 | api.fda.gov |
| indigodental GmbH | Pinneberg Schleswig-Holstein, Germany | Exporter to the US, Manufacturer | 4 | September 30, 2016 | 0 | 0 | 0 | api.fda.gov |
| Deltamed GMBH | FRIEDBERG Hesse, Germany | Manufacturer | 3 | July 24, 2024 | 0 | 0 | 0 | api.fda.gov |
| DENTSPLY DETREY GmbH | KONSTANZ Baden-Wurttemberg, Germany | Manufacturer | 1 | February 28, 1978 | 0 | 0 | 0 | api.fda.gov |
| Detax GMBH | ETTLINGEN Baden-Wurttemberg, Germany | Manufacturer | 1 | July 23, 2010 | 0 | 0 | 0 | api.fda.gov |
| Hager & Werken GMBH | DUISBURG,DE-NOTA Hamburg, Germany | Manufacturer | 1 | May 27, 2005 | 0 | 0 | 0 | api.fda.gov |
| Kettenbach GMBH & Co KG | ESCHENBURG Hesse, Germany | Manufacturer | 1 | November 8, 2019 | 0 | 0 | 0 | api.fda.gov |
| Dreve Dentamid GMBH | UNNA North Rhine-Westphalia, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Identa Dental Material GMBH | CUXHAVEN Lower Saxony, 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.