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

Claripi, Inc. has 4 FDA 510(k) cleared medical devices. Based in Seoul, KR.

Last cleared in 2022. Active since 2019. Primary specialty: Radiology.

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

Regulatory submissions have been managed by Claripi Detroit Office and Claripi USA, Inc..