Denti.Ai Technology, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Denti.Ai Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Denti.AI Detect, Denti.AI Auto-Chart
2
Total
2
Cleared
0
Denied
Denti.Ai Technology, Inc. has 2 FDA 510(k) cleared medical devices. Based in Toronto, CA.
Last cleared in 2023. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Denti.Ai Technology, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Biologics Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Denti.Ai Technology, Inc.
2 devices