Mebo Life Science, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Mebo Life Science, Inc. has 2 FDA 510(k) cleared medical devices. Based in Brea, US.
Last cleared in 2022. Active since 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Mebo Life Science, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Vee Care (Asia) Limited as regulatory consultant.
2 devices