Provect.AI is one of 12989 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Provect.AI - FDA 510(k) Cleared Devices
Recent clearances: 3D-Anywhere
1
Total
1
Cleared
0
Denied
Provect.AI has 1 FDA 510(k) cleared medical devices. Based in Los Gatos, US.
Latest FDA clearance: Jul 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Provect.AI Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ProMedic Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Provect.AI
1 devices