Medical Device Manufacturer · CN , Hong Kong

Kenpax International Limited - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2021

Total

Cleared

Denied

Kenpax International Limited has 4 FDA 510(k) cleared medical devices. Based in Hong Kong, CN.

Last cleared in 2023. Active since 2021. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Kenpax International Limited Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Kenpax International Limited

4 devices

1-4 of 4