Medical Device Manufacturer · CN , Shenzhen

Shenzhen Kaiyan Medical CO , Ltd. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2021

Total

Cleared

Denied

Shenzhen Kaiyan Medical CO , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.

Last cleared in 2022. Active since 2021. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Shenzhen Kaiyan Medical CO , Ltd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Guangzhou GLOMED Biological Technology Co., Ltd. as regulatory consultant.

Shenzhen Kaiyan Medical CO , Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Shenzhen Kaiyan Medical CO , Ltd.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 19, 2026