Neurovice, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neurovice, LLC - FDA 510(k) Cleared Devices
Recent clearances: PATI (Protector Against Tongue Injury)
1
Total
1
Cleared
0
Denied
Neurovice, LLC has 1 FDA 510(k) cleared medical devices. Based in Wake Forest, US.
Last cleared in 2023. Active since 2023. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neurovice, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Gilero, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Neurovice, LLC
1 devices