Paige.Ai is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Paige.Ai - FDA 510(k) Cleared Devices
1
Total
0
Cleared
1
Denied
Paige.Ai has 0 FDA 510(k) cleared medical devices. Based in New York, US.
Active since 2021. Primary specialty: Pathology.
Browse the FDA 510(k) cleared devices submitted by Paige.Ai Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Paige.Ai
1 devices