Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)
Mar 2026
202d
Myofunctional Research Co.
1
Total
1
Cleared
0
Denied
Myofunctional Research Co. — FDA 510(k) Submissions
Myofunctional Research Co. has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Device, Anti-snoring . Use the specialty filter in the sidebar to narrow results.
1 devices