Data / Medical devices / Light-Induced Fluorescence Caries Detector / Germany
FDA-registered makers of Light-Induced Fluorescence Caries Detector in Germany: 5 establishments
5 establishments in Germany are registered with the FDA to make Light-Induced Fluorescence Caries Detector (product code NBL). 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
- Light-Induced Fluorescence Caries Detector
- Product code
- NBL
- Country
- Germany
Makers of Light-Induced Fluorescence Caries Detector 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 | 2 | August 2, 2005 | 0 | 0 | 0 | api.fda.gov |
| Durr Dental Se | Bietigheim-Bissingen Baden-Wurttemberg, Germany | Complaint file establishment, Specification developer | 1 | January 27, 2016 | 0 | 0 | 0 | api.fda.gov |
| Durr Optronik GmbH & Co. KG | Gechingen Baden-Wurttemberg, Germany | Manufacturer | 1 | January 27, 2016 | 0 | 0 | 0 | api.fda.gov |
| JENOPTIK Optical Systems GmbH | Berlin, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sirona Dental Systems GMBH | BENSHEIM Hesse, Germany | 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.