Unicoglobal, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Unicoglobal, Inc. has 2 FDA 510(k) cleared medical devices. Based in Seongnam, KR.
Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Unicoglobal, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.
2 devices