LVIS Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
LVIS Corporation - FDA 510(k) Cleared Devices
Recent clearances: NeuroMatch, NeuroMatch, LVIS NeuroMatch
3
Total
3
Cleared
0
Denied
LVIS Corporation has 3 FDA 510(k) cleared medical devices. Based in Palo Alto, US.
Latest FDA clearance: May 2025. Active since 2023. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by LVIS Corporation Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mcra, LLC and Veranex, Inc..
FDA 510(k) Regulatory Record - LVIS Corporation
3 devices