Medical Device Manufacturer · US , Santa Fe Springs , CA

Lumenessa Corp - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023
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.

FDA 510(k) cleared devices by Lumenessa Corp

1 devices
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