Ultromics Limited is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Ultromics Limited - FDA 510(k) Cleared Devices
Recent clearances: EchoGo Amyloidosis (1.0), EchoGo Heart Failure (2.0), EchoGo Heart Failure
4
Total
4
Cleared
0
Denied
Ultromics Limited has 4 FDA 510(k) cleared medical devices. Based in Oxford, GB.
Latest FDA clearance: Nov 2024. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ultromics Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ultromics Limited
4 devices