Mgnewton , Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Mgnewton , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ELEC Master, ELEC Master Dual, CURA-Temp
2
Total
2
Cleared
0
Denied
Mgnewton , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Gyeongsan-Si, KR.
Last cleared in 2023. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Mgnewton , 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 - Mgnewton , Ltd.
2 devices