Bryan Medical, Inc. is one of 16529 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bryan Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Tenax® Laser Resistant Endotracheal Tube, Tenax Laser Resistant Endotracheal Tube, Tenax Laser Resistant Endotracheal Tube
4
Total
4
Cleared
0
Denied
Bryan Medical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Cincinnati, US.
Latest FDA clearance: Sep 2026. Active since 2015. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Bryan Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by AlvaMed, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Bryan Medical, Inc.
4 devices
Cleared
Sep 03, 2026
Tenax® Laser Resistant Endotracheal Tube
Anesthesiology
448d
Cleared
Oct 21, 2021
Tenax Laser Resistant Endotracheal Tube
Anesthesiology
30d
Cleared
Nov 25, 2020
Tenax Laser Resistant Endotracheal Tube
Anesthesiology
246d
Cleared
Jun 25, 2015
aeris Balloon Dialation Catheter
Ear, Nose, Throat
77d