PanopticAI technologies Limited is one of 14 FDA 510(k) medical device manufacturers from Hong Kong in the dataset, ranked by real submission volume.
PanopticAI technologies Limited - FDA 510(k) Cleared Devices
Recent clearances: PanopticAI Vital Signs (1.6.1-22), PanopticAI Vital Signs
2
Total
2
Cleared
0
Denied
PanopticAI technologies Limited has 2 FDA 510(k) cleared medical devices. Based in Hong Kong, HK.
Latest FDA clearance: May 2026. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by PanopticAI technologies Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Vee Care (Asia) Limited as regulatory consultant.
FDA 510(k) Regulatory Record - PanopticAI technologies Limited
2 devices