Syntheon - FDA 510(k) Cleared Devices

Syntheon has 1 FDA 510(k) cleared medical devices. Based in Miami, US.

Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Syntheon Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Caraballo Consulting, LLC as regulatory consultant.