Venis DI A. Vendrame
ItalyFDA applicant, unverified
- Devices
- 1
What Venis DI A. Vendrame makes
Venis DI A. Vendrame manufactures spectacle frames, which are optical devices designed to support eyeglasses lenses for vision correction or protection.
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 K930435
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Venis DI A. Vendrame have in the registry?
The registry currently lists 1 device for Venis DI A. Vendrame. Devices recorded under merged duplicate company entries are counted once.
Which registries list Venis DI A. Vendrame's devices?
Among its 1 most recently registered device, Venis DI A. Vendrame has devices listed in FDA 510(k) (1 device).
What risk classes do Venis DI A. Vendrame's devices fall under?
Among its 1 most recently registered device, the classes recorded for Venis DI A. Vendrame's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Venis DI A. Vendrame in the registry?
The most recently registered devices listed for Venis DI A. Vendrame include SPECTACLE FRAMES.