Medical Device Manufacturer · CN , Shenzhen

Shenzhen Desida Technology Co., Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2022

Total

Cleared

Denied

Shenzhen Desida Technology Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.

Latest FDA clearance: Mar 2026. Active since 2022. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Shenzhen Desida Technology Co., Ltd. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Feiying Drug & Medical Consulting Technical Service Group and Shenzhen CT Bio-Tech Co., Ltd..

Shenzhen Desida Technology 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 Desida Technology Co., Ltd.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,730 total devices indexed.

Last updated: Apr 27, 2026