Biomed Ent, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biomed Ent, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Epi-Stop Nasal Gel/epistaxis pack
1
Total
1
Cleared
0
Denied
Biomed Ent, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Last cleared in 2023. Active since 2023. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Biomed Ent, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Biomed Elements B.V. as regulatory consultant.
FDA 510(k) Regulatory Record - Biomed Ent, Inc.
1 devices