Medo.Ai is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Medo.Ai - FDA 510(k) Cleared Devices
Recent clearances: MEDO ARIA
1
Total
1
Cleared
0
Denied
Medo.Ai has 1 FDA 510(k) cleared medical devices. Based in Edmonton, CA.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Medo.Ai Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medo.Ai
1 devices