Medical Device Manufacturer · CN , Wuhan

Wuhan Pioon Technology Co., Ltd. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2023

Total

Cleared

Denied

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

Latest FDA clearance: May 2025. Active since 2023. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by leanRAQA as regulatory consultant.

FDA 510(k) Regulatory Record - Wuhan Pioon 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 30, 2026