Dio Medical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dio Medical Corp. - FDA 510(k) Cleared Devices
Recent clearances: Huvex Interspinous Fusion System
1
Total
1
Cleared
0
Denied
Dio Medical Corp. has 1 FDA 510(k) cleared medical devices. Based in East Norriton, US.
Last cleared in 2023. Active since 2023. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Dio Medical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dio Medical Corp.
1 devices