Kenpax International Limited is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Kenpax International Limited - FDA 510(k) Cleared Devices
Recent clearances: Protective Gown AAMI Level 4, Sterilization Wrap, Isolation Gown AAMI Level 3
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 Shenzhen Joyantech Consulting Co., Ltd., Beijing Believe-Med Technology Service Co., Ltd. and Shanghai Sungo Management Consulting Company Limited..
FDA 510(k) Regulatory Record - Kenpax International Limited
4 devices