Medical Device Manufacturer · KR , Gimhae-Si

Dk Mungyo Corporation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2020

Recent clearances: Flex Fit

1
Total
1
Cleared
0
Denied

Dk Mungyo Corporation has 1 FDA 510(k) cleared medical devices. Based in Gimhae-Si, KR.

Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Dk Mungyo Corporation 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 - Dk Mungyo Corporation

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