Vita
Country not established
- Devices
- 1
What Vita makes
Vita manufactures dental CAD/CAM systems designed for in-lab use, including the VITA CAD-TEMP series (models VX59-4002, VX59-4010, VX59-4102, VX59-4110, VX59-4202, VX59-4210, VX59-4302, VX59-4310) for temporary crown and bridge fabrication.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vita have in the registry?
The registry currently lists 1 device for Vita. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vita's devices?
Among its 1 most recently registered device, Vita has devices listed in FDA 510(k) (1 device).
What risk classes do Vita's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vita's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vita in the registry?
The most recently registered devices listed for Vita include VITA CAD-TEMP FOR INLAB, MODEL, VX59-4002, VX59-4010, VX59-4102, VX59-4110, VX59-4202, VX59-4210, VX59-4302, VX59-4310.