Ceryn? Intimate Care
Dec 2025
296d
Ansella Therapeutics
1
Total
1
Cleared
0
Denied
Ansella Therapeutics — FDA 510(k) Submissions
Ansella Therapeutics 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 Lubricant, Personal . Use the specialty filter in the sidebar to narrow results.
1 devices