Data / Medical devices / Controller, Foot, Handpiece And Cord / Germany
FDA-registered makers of Controller, Foot, Handpiece And Cord in Germany: 5 establishments
5 establishments in Germany are registered with the FDA to make Controller, Foot, Handpiece And Cord (product code EBW). 5 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
- Controller, Foot, Handpiece And Cord
- Product code
- EBW
- Country
- Germany
Makers of Controller, Foot, Handpiece And Cord in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Kavo Dental GMBH | WARTHAUSEN Baden-Wurttemberg, Germany | Manufacturer | 3 | February 21, 2017 | 0 | 0 | 0 | api.fda.gov |
| Kavo Dental GMBH | BIBERACH Baden-Wurttemberg, Germany | Specification developer | 1 | February 21, 2017 | 0 | 0 | 0 | api.fda.gov |
| Sirona Dental Systems GMBH | BENSHEIM Hesse, Germany | Manufacturer | 1 | August 25, 2025 | 0 | 0 | 0 | api.fda.gov |
| Sycotec GMBH & Co KG | Leutkirch Baden-Wurttemberg, Germany | Contract manufacturer, Manufacturer | 1 | July 24, 2009 | 0 | 0 | 0 | api.fda.gov |
| Sirona Dental Systems GmbH | Bensheim Hesse, Germany | Specification developer | 1 | May 3, 2006 | 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.