DentMedi Co., Ltd. is one of 468 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
DentMedi Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: INNI-CERA (BCM-W500, BCM-W1000)
1
Total
1
Cleared
0
Denied
DentMedi Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Gunposi, KR.
Latest FDA clearance: Oct 2026. Active since 2026. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by DentMedi Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by E & M as regulatory consultant.
FDA 510(k) Regulatory Record - DentMedi Co., Ltd.
1 devices