Epi-Stop Nasal Gel/epistaxis pack
Mar 2023
63d
Biomed Ent, Inc.
1
Total
1
Cleared
0
Denied
Biomed Ent, Inc. — FDA 510(k) Submissions
Biomed Ent, Inc. has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Splint, Intranasal Septal . Use the specialty filter in the sidebar to narrow results.
1 devices