PulseAI, Ltd. is one of 520 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
PulseAI, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: PulseAPI SmartWatch
1
Total
1
Cleared
0
Denied
PulseAI, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Belfast, GB.
Latest FDA clearance: Oct 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by PulseAI, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - PulseAI, Ltd.
1 devices