Vista AI, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vista AI, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Vista OS, Vista AI Scan, RTHawk
1
Total
1
Cleared
0
Denied
Vista AI, Inc. has 1 FDA 510(k) cleared medical devices. Based in Palo Alto, US.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Vista AI, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Heartvista, Inc. Dba Vista.Ai as regulatory consultant.
FDA 510(k) Regulatory Record - Vista AI, Inc.
1 devices