Venis DI Alessandro Vendrame
ItalyFDA applicant, unverified
- Devices
- 1
What Venis DI Alessandro Vendrame makes
Venis DI Alessandro Vendrame manufactures spectacle frames, which are designed for optical correction and aesthetic use in eyeglasses.
The company’s spectacle frames are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Spectacle Frames Ref K930597
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Venis DI Alessandro Vendrame have in the registry?
The registry currently lists 1 device for Venis DI Alessandro Vendrame. Devices recorded under merged duplicate company entries are counted once.
Which registries list Venis DI Alessandro Vendrame's devices?
Among its 1 most recently registered device, Venis DI Alessandro Vendrame has devices listed in FDA 510(k) (1 device).
What risk classes do Venis DI Alessandro Vendrame's devices fall under?
Among its 1 most recently registered device, the classes recorded for Venis DI Alessandro Vendrame's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Venis DI Alessandro Vendrame in the registry?
The most recently registered devices listed for Venis DI Alessandro Vendrame include SPECTACLE FRAMES.