Visiodent SA
Country not established
- Devices
- 1
What Visiodent SA makes
Visiodent SA manufactures the Visiodent Radiology System, a device designed for dental imaging to capture intraoral radiographs, enabling precise visualization of teeth and surrounding structures for diagnostic purposes.
The Visiodent Radiology System is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Rsv (Radiology System Visiodent Ref K031448
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Visiodent SA have in the registry?
The registry currently lists 1 device for Visiodent SA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Visiodent SA's devices?
Among its 1 most recently registered device, Visiodent SA has devices listed in FDA 510(k) (1 device).
What risk classes do Visiodent SA's devices fall under?
Among its 1 most recently registered device, the classes recorded for Visiodent SA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Visiodent SA in the registry?
The most recently registered devices listed for Visiodent SA include RSV (RADIOLOGY SYSTEM VISIODENT.