Lumenessa Corp - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Lumenessa Corp has 1 FDA 510(k) cleared medical devices. Based in Santa Fe Springs, US.
Last cleared in 2023. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lumenessa Corp Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Delta Technology Service(Shenzhen) Co., Ltd. as regulatory consultant.
1 devices