Endurance Therapeutics is one of 200 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Endurance Therapeutics - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Endurance Therapeutics has 2 FDA 510(k) cleared medical devices. Based in Dauphin, Manitoba, CA.
Historical record: 2 cleared submissions from 2007 to 2013. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Endurance Therapeutics Filter by specialty or product code using the sidebar.
Endurance Therapeutics — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jul 19, 2013
T1040 AKA AURAWAVE
Neurology
200d
Cleared
Dec 03, 2007
THERAPEUTIC MASSAGE COMPANION
Neurology
615d