Neurovalens , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Neurovalens , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Modius Sleep
1
Total
1
Cleared
0
Denied
Neurovalens , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Portglenone, GB.
Last cleared in 2023. Active since 2023. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neurovalens , Ltd. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Neurovalens , Ltd.
1 devices