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

Adcura, Inc. has 1 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.

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

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

510(k) submissions have been managed by Empirical Technologies as regulatory consultant.