Curexo, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Curexo, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CUVIS-joint (CJ150), CUVIS-spine, CUVIS-spine
4
Total
4
Cleared
0
Denied
Curexo, Inc. has 4 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Mar 2026. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Curexo, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bt Solutions, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Curexo, Inc.
4 devices