Medical Device Manufacturer · US , Leesburg , FL

Ya-Man, Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2001

Total

Cleared

Denied

Ya-Man, Ltd. has 6 FDA 510(k) cleared medical devices. Based in Leesburg, US.

Latest FDA clearance: Oct 2025. Active since 2001. Primary specialty: Neurology.

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

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.

Ya-Man, 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 - Ya-Man, Ltd.

6 devices

1-6 of 6

Data Source

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

Last updated: Apr 27, 2026