Not currently registered with FDA under this name
Vita
Brea, CA, United States. Named as applicant on 1 dental 510(k) clearance between 2007 and 2007. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 12007–2007
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2000–2026
510(k) clearances
Clearances on which FDA names Vita as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 1 Jun 2007 | K070991 | VITA CAD-TEMP FOR INLAB, MODEL, VX59-4002, VX59-4010, VX59-4102, VX59-4110, VX59-4202, VX59-4210, VX59-4302, VX59-4310 | EBG Resin Temporary Crown and Bridge |
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.