Dio Medical Corporation - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Dio Medical Corporation has 4 FDA 510(k) cleared medical devices. Based in East Norriton, US.
Last cleared in 2022. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Dio Medical Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Dio Medical Corporation
4 devices
Cleared
Oct 25, 2022
Rexious Spinal Fixation System
Orthopedic
76d
Cleared
Oct 18, 2022
FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate...
Orthopedic
54d
Cleared
Oct 13, 2022
UNITY Sacroiliac Joint Fixation System
Orthopedic
59d
Cleared
Oct 05, 2022
FaSet Fixation System
Orthopedic
47d