Medical Device Manufacturer · US , Santee , CA

Techna Vision

4 submissions · 4 cleared · Since 1985
4
Total
4
Cleared
0
Denied

Techna Vision — FDA 510(k) Submissions

Techna Vision has submitted 4 FDA 510(k) premarket notifications since 1985, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Perimeter, Automatic, Ac-powered, Chair, Ophthalmic, Ac-powered, Table, Instrument, Powered, Ophthalmic, Lens, Spectacle, Non-custom (prescription) . Use the specialty filter in the sidebar to narrow results.

4 devices
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All4 Ophthalmic 4