Avicena, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Avicena, LLC - FDA 510(k) Cleared Devices
Recent clearances: Vivio® LVEDP System, Vivio System
2
Total
2
Cleared
0
Denied
Avicena, LLC has 2 FDA 510(k) cleared medical devices. Based in Altadena, US.
Last cleared in 2023. Active since 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Avicena, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by West Device Innovations and Qserve Group US.
FDA 510(k) Regulatory Record - Avicena, LLC
2 devices