NewVision SC (tisilfocon A) Scleral Lens; NewVision SC Daily Wear Ortho-K (tisilfocon A) Corneo-Scleral Lens
Jun 2023
77d
Acculens, Inc.
1
Total
1
Cleared
0
Denied
Acculens, Inc. — FDA 510(k) Submissions
Acculens, Inc. has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Lens, Contact (other Material) - Daily . Use the specialty filter in the sidebar to narrow results.
1 devices