Cruxell Corp. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Cruxell Corp. - FDA 510(k) Cleared Devices
Recent clearances: CRUXVIEW, Cruxcan (CRX-1000)
2
Total
2
Cleared
0
Denied
Cruxell Corp. has 2 FDA 510(k) cleared medical devices. Based in Daejeon, KR.
Last cleared in 2021. Active since 2019. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Cruxell Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Cruxell Corp.
2 devices