Medical Device Manufacturer · US , Great Neck , NY

Dxm Co., Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2004

Total

Cleared

Denied

Dxm Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Great Neck, US.

Historical record: 6 cleared submissions from 2004 to 2020. Primary specialty: Dental.

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

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

Dxm Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Dxm Co., Ltd.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: May 28, 2026