Visard SRL
ItalyFDA applicant, unverified FDA FEI 1000322593
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Visard SRL makes
Visard Srl manufactures prescription and non-prescription sunglasses designed for UV protection and general eyewear use. The products include standard sunglasses and specialized visard sunglasses, which are likely intended for occupational or high-visibility applications.
The company’s portfolio is classified under FDA’s Class I medical devices and is listed in the 510(k) registry. These devices are regulated under the US jurisdiction, where Visard Srl is based.
Catalogue
Visard Sunglasses Ref K961117
Regimes: 510(k) Registry: 510(k)Sunglasses Ref K960818
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000322593
- Address
- VIA FELTRINA 18, QUERO BELLUNO
Frequently asked questions
How many devices does Visard Srl have in the registry?
The registry currently lists 2 devices for Visard Srl. Devices recorded under merged duplicate company entries are counted once.
Which registries list Visard Srl's devices?
Among its 2 most recently registered devices, Visard Srl has devices listed in FDA 510(k) (2 devices).
What risk classes do Visard Srl's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Visard Srl's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Visard Srl in the registry?
The most recently registered devices listed for Visard Srl include VISARD SUNGLASSES and SUNGLASSES.