Dmax Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Dmax Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Multi M Series, DMAX Coloring Liquid
2
Total
2
Cleared
0
Denied
Dmax Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Daegu, KR.
Latest FDA clearance: Jun 2025. Active since 2018. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dmax Co., Ltd. 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 - Dmax Co., Ltd.
2 devices