Polarisar, Inc. - FDA 510(k) Cleared Devices

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

Last cleared in 2023. Active since 2023. Primary specialty: Orthopedic.

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

510(k) submissions have been managed by MEDIcept, Inc. as regulatory consultant.