Medical Device Manufacturer · US , Kennewick , WA

Tisport, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

Total

Cleared

Denied

Tisport, LLC has 2 FDA 510(k) cleared medical devices. Based in Kennewick, US.

Historical record: 2 cleared submissions from 2002 to 2007. Primary specialty: Physical Medicine.

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

Tisport, LLC 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, LLC

2 devices

1-2 of 2