Remvia NightGuard
Dec 2025
269d
Remvia
1
Total
1
Cleared
0
Denied
Remvia — FDA 510(k) Submissions
Remvia has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Mouthguard, Prescription . Use the specialty filter in the sidebar to narrow results.
1 devices