Vista Vision
Country not established
- Devices
- 1
What Vista Vision makes
Vista Vision manufactures The Visonic Dome™, a medical device designed for retinal imaging and examination, enabling detailed visualization of the eye’s posterior segment.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance for market authorization. The device is listed in the FDA’s 510(k) database. Vista Vision operates from the United States.
Catalogue
The Visonic Dome(Tm) Ref K902306
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vista Vision have in the registry?
The registry currently lists 1 device for Vista Vision. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vista Vision's devices?
Among its 1 most recently registered device, Vista Vision has devices listed in FDA 510(k) (1 device).
What risk classes do Vista Vision's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vista Vision's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vista Vision in the registry?
The most recently registered devices listed for Vista Vision include THE VISONIC DOME(TM).