LVIS Corporation - FDA 510(k) Cleared Devices

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..