Medical Device Manufacturer · KR , Cheonan-Si

Dentalmax Co., Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2018
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
1-3 of 3
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All3 Dental 3