Not currently registered with FDA under this name
Vita Zanhnfabrik H. Rauter GmbH Co.
Bad Sackingen, Germany. Named as applicant on 1 dental 510(k) clearance between 2020 and 2020. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 12020–2020
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2007–2026
510(k) clearances
Clearances on which FDA names Vita Zanhnfabrik H. Rauter GmbH Co. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 29 Jan 2020 | K191926 | VITA VIONIC Bond | EBI Rebasing Repairing Relining Denture Resin |
Some of these clearances are listed with FDA today by another company: Vita Zahnfabrik H. Rauter GmbH & Co. Kg. (1).
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.