Claripi, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Claripi, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ClariPulmo, ClariSIGMAM, ClariCT.AI
4
Total
4
Cleared
0
Denied
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, O Tech, Inc. and Claripi USA, Inc..
FDA 510(k) Regulatory Record - Claripi, Inc.
4 devices