Neuhealth Digital , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Neuhealth Digital , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Neu Platform
1
Total
1
Cleared
0
Denied
Neuhealth Digital , Ltd. has 1 FDA 510(k) cleared medical devices. Based in London, GB.
Latest FDA clearance: Apr 2025. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neuhealth 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 - Neuhealth Digital , Ltd.
1 devices