Outlook Surgical Versa One System (8900139)
Aug 2025
420d
Resnent, LLC
1
Total
1
Cleared
0
Denied
Resnent, LLC — FDA 510(k) Submissions
Resnent, LLC 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 Nasopharyngoscope (flexible Or Rigid) . Use the specialty filter in the sidebar to narrow results.
1 devices