Medical Device Manufacturer · US , Altadena , CA

Avicena, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2019
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.

510(k) submissions have been managed by Qserve Group US as regulatory consultant.

FDA 510(k) Regulatory Record - Avicena, LLC
2 devices
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