Visionary Optics, LLC
United Statesfrom the FDA registration address FDA establishment FEI 1000123221
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Visionary Optics Scleral Contact Lens (roflufocon D, roflufocon E, hexafocon A, hexafocon B) Ref K171950
Regimes: 510(k) Registry: 510(k)Visionary Optics Scleral Contact Lens (roflufocon D, roflufocon E, hexafocon A, hexafocon B, tisilfocon A) Ref K223394
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000123221
- Address
- 1325 Progress Drive, Front Royal, VA, 22630
Frequently asked questions
How many devices does Visionary Optics, LLC have in the registry?
The registry currently lists 3 devices for Visionary Optics, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Visionary Optics, LLC's devices?
Among its 3 most recently registered devices, Visionary Optics, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Visionary Optics, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Visionary Optics, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Visionary Optics, LLC in the registry?
The most recently registered devices listed for Visionary Optics, LLC include Visionary Optics Scleral Contact Lens (roflufocon D, roflufocon E, hexafocon A, hexafocon B), Visionary Optics Scleral Contact Lens (roflufocon D, roflufocon E, hexafocon A, hexafocon B, tisilfocon A) and Visionary Optics Scleral Contact Lens (roflufocon D, roflufocon E, hexafocon A, hexafocon B, tisilfocon A, fluoroxyfocon A).