Kenpax International Limited - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
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.
Regulatory submissions have been managed by Shanghai Sungo Management Consulting Company Limited., Shenzhen Joyantech Consulting Co., Ltd. and Beijing Believe-Med Technology Service Co., Ltd..
4 devices