Bryan Medical, Inc. is one of 5511 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
3
Total
3
Cleared
0
Denied
Bryan Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Cincinnati, US.
Last cleared in 2021. 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.
3 devices