Dentalmax Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Dentalmax Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: LUXEN 5G, LUXEN CL Dental Liquid, LUXEN Zr, LUXEN Smile
3
Total
3
Cleared
0
Denied
Dentalmax Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Cheonan-Si, KR.
Latest FDA clearance: Sep 2024. Active since 2018. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dentalmax 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 - Dentalmax Co., Ltd.
3 devices