Medical Device Manufacturer · US , Stevens Point , WI

Ki Mobility, LLC - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2006

Total

Cleared

Denied

Ki Mobility, LLC has 5 FDA 510(k) cleared medical devices. Based in Stevens Point, US.

Last cleared in 2023. Active since 2006. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Ki Mobility, LLC Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.

Ki Mobility, LLC is one of 16306 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ki Mobility, LLC

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: May 15, 2026