Medical Device Manufacturer · US , Kennewick , WA

Tisport - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1999

Total

Cleared

Denied

Tisport has 5 FDA 510(k) cleared medical devices. Based in Kennewick, US.

Historical record: 5 cleared submissions from 1999 to 2002. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Tisport Filter by specialty or product code using the sidebar.

Tisport 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 - Tisport

5 devices

1-5 of 5

Data Source

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

Last updated: Apr 27, 2026