Data / Medical devices / Powder, Porcelain / Germany
FDA-registered makers of Powder, Porcelain in Germany: 12 establishments
12 establishments in Germany are registered with the FDA to make Powder, Porcelain (product code EIH). 11 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Powder, Porcelain
- Product code
- EIH
- Country
- Germany
Makers of Powder, Porcelain in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Vita Zahnfabrik H. Rauter GMBH & Co. KG. | BAD SACKINGEN Baden-Wurttemberg, Germany | Manufacturer, Repackager or relabeler | 25 | February 21, 2025 | 0 | 0 | 0 | api.fda.gov |
| Degudent GMBH | HANAU Hesse, Germany | Exporter to the US, Manufacturer, Specification developer | 14 | October 24, 2024 | 0 | 0 | 0 | api.fda.gov |
| Dental Direkt GmbH | Spenge North Rhine-Westphalia, Germany | Contract manufacturer, Manufacturer, Repackager or relabeler | 7 | September 6, 2024 | 0 | 0 | 0 | api.fda.gov |
| etkon GMBH | Markkleeberg Saxony, Germany | Manufacturer | 6 | November 14, 2017 | 0 | 0 | 0 | api.fda.gov |
| Pritidenta GMBH | Leinfelden-Echterdingen Baden-Wurttemberg, Germany | Exporter to the US, Foreign private label distributor, Manufacturer | 3 | February 3, 2017 | 0 | 0 | 0 | api.fda.gov |
| Sirona Dental Systems GMBH | BENSHEIM Hesse, Germany | Exporter to the US, Specification developer | 3 | August 1, 2018 | 0 | 0 | 0 | api.fda.gov |
| Solventum Germany GmbH | SEEFELD Bavaria, Germany | Manufacturer | 3 | September 1, 2016 | 0 | 0 | 0 | api.fda.gov |
| Dentaurum GmbH & Co. KG | ISPRINGEN Baden-Wurttemberg, Germany | Manufacturer | 2 | June 5, 2001 | 0 | 0 | 0 | api.fda.gov |
| Whitepeaks Dental Solutions GMBH | Hamminkeln North Rhine-Westphalia, Germany | Manufacturer | 2 | February 21, 2013 | 0 | 0 | 0 | api.fda.gov |
| Creamed GMBH & Co. Produktions- Und Handels KG | Marburg Hesse, Germany | Manufacturer | 1 | September 24, 2013 | 0 | 0 | 0 | api.fda.gov |
| Yeti Dentalprodukte GMBH | Engen Baden-Wurttemberg, Germany | Manufacturer | 1 | November 15, 2018 | 0 | 0 | 0 | api.fda.gov |
| Degudent GMBH | Rosbach V.D.H. Hesse, 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.