C.E.I.B.Med is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
C.E.I.B.Med - FDA 510(k) Cleared Devices
Recent clearances: Reon
1
Total
1
Cleared
0
Denied
C.E.I.B.Med has 1 FDA 510(k) cleared medical devices. Based in Seoul-Si, KR.
Latest FDA clearance: May 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by C.E.I.B.Med Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by GMSC Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - C.E.I.B.Med
1 devices