Rhythm AI, Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Rhythm AI, Ltd. has 2 FDA 510(k) cleared medical devices. Based in London, GB.
Latest FDA clearance: Dec 2025. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Rhythm AI, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Rhythm AI, Ltd.
2 devices