Rebound Therapeutics Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rebound Therapeutics Corporation - FDA 510(k) Cleared Devices
Recent clearances: Aurora Surgiscope System, Aurora Surgiscope System
2
Total
2
Cleared
0
Denied
Rebound Therapeutics Corporation has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.
Last cleared in 2023. Active since 2019. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Rebound Therapeutics Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rebound Therapeutics Corporation
2 devices