Medical Device Manufacturer · FR , Paris

Mauna Kea Technologies - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 2005
18
Total
18
Cleared
0
Denied

Mauna Kea Technologies has 18 FDA 510(k) cleared general & plastic surgery devices. Based in Paris, FR.

Last cleared in 2022. Active since 2005.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Mauna Kea Technologies

18 devices
1-12 of 18
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