DIMPLO, Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
DIMPLO, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: DIMPLO Implant System
1
Total
1
Cleared
0
Denied
DIMPLO, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Busan, KR.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by DIMPLO, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - DIMPLO, Ltd.
1 devices