Not currently registered with FDA under this name
Duerr Dental AG
Bietigheim-Bissingen, Germany. Named as applicant on 2 dental 510(k) clearances between 2017 and 2017. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 22017–2017
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2007–2026
510(k) clearances
Clearances on which FDA names Duerr Dental AG as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 22 Nov 2017 | K172007 | CamX Triton HD Proxi Head | NTK Light Transmission Caries Detector |
| 1 May 2017 | K170733 | ScanX Intraoral View | MUH Digital Extraoral Source X-Ray System |
Some of these clearances are listed with FDA today by another company: Durr Dental SE (2).
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.