Data / Medical devices / Activator, Ultraviolet, For Polymerization / Germany
FDA-registered makers of Activator, Ultraviolet, For Polymerization in Germany: 5 establishments
5 establishments in Germany are registered with the FDA to make Activator, Ultraviolet, For Polymerization (product code EBZ). 3 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
- Activator, Ultraviolet, For Polymerization
- Product code
- EBZ
- Country
- Germany
Makers of Activator, Ultraviolet, For Polymerization in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Kulzer GMBH | HANAU Hesse, Germany | Exporter to the US, Specification developer | 3 | December 7, 2009 | 0 | 0 | 0 | api.fda.gov |
| Solventum Germany GmbH | SEEFELD Bavaria, Germany | Manufacturer, Repackager or relabeler, Specification developer | 3 | May 16, 2001 | 0 | 0 | 0 | api.fda.gov |
| DENTSPLY DETREY GmbH | KONSTANZ Baden-Wurttemberg, Germany | Manufacturer | 1 | June 24, 2004 | 0 | 0 | 0 | api.fda.gov |
| Kulzer GMBH | WEHRHEIM Hesse, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Schott AG | Mainz Rhineland-Palatinate, 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.