Kneu Health Digital , Ltd. is one of 386 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Kneu Health Digital , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Kneu Platform (V2)
1
Total
1
Cleared
0
Denied
Kneu Health Digital , Ltd. has 1 FDA 510(k) cleared medical devices. Based in London, GB.
Latest FDA clearance: Aug 2026. Active since 2026. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Kneu Health Digital , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Kneu Health Digital , Ltd.
1 devices