Rebound Therapeutics - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Rebound Therapeutics has 6 FDA 510(k) cleared medical devices. Based in Irvine, US.
Last cleared in 2021. Active since 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Rebound Therapeutics Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Rebound Therapeutics
6 devices
Cleared
Dec 02, 2021
AURORA Evacuator +Coag
Neurology
345d
Cleared
Nov 04, 2020
Aurora Surgiscope System (Surgiscope), Aurora Surgiscope System (Image...
Neurology
125d
Cleared
Aug 12, 2020
Aurora Evacuator +Coag
General & Plastic Surgery
57d
Cleared
Dec 06, 2019
Aurora Surgiscope System
Neurology
148d
Cleared
Feb 12, 2019
Aurora Evacuator
General & Plastic Surgery
27d
Cleared
Apr 09, 2018
Aurora Evacuator
General & Plastic Surgery
56d