Medical Device Manufacturer · CN , Shenzhen

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

7 submissions · 7 cleared · Since 2020

Total

Cleared

Denied

Shenzhen Leaflife Technology Co., Ltd. has 7 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.

Latest FDA clearance: Nov 2025. Active since 2020. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Aestheticcert Compliance, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Shenzhen Leaflife Technology Co., Ltd.

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 27, 2026