Medical Device Manufacturer · CN , Beijing

Beijing Globalipl Development Co., Ltd. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2020

Total

Cleared

Denied

Beijing Globalipl Development Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Beijing, CN.

Last cleared in 2022. Active since 2020. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Beijing Globalipl Development Co., Ltd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Beijing Believe-Med Technology Service Co., Ltd. as regulatory consultant.

Beijing Globalipl Development 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 - Beijing Globalipl Development Co., Ltd.

4 devices

1-4 of 4

Data Source

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

Last updated: May 19, 2026