OdneClean
Aug 2024
248d
Odne AG
1
Total
1
Cleared
0
Denied
Odne AG — FDA 510(k) Submissions
Odne AG has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Scaler, Ultrasonic . Use the specialty filter in the sidebar to narrow results.
1 devices