# Tisport

- Location (FDA's records): Kennewick, WA
- FDA decisions: 7 (1999–2007): 7 510(k) clearances
- Names in FDA's records: Tisport (5); Tisport, LLC (2)
- Product codes: IOR (5), ITI (2)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Motion Designs, Inc.: 3 (https://510kreport.com/company/motion-designs)
- Fortress Lite-Style Wheelchairs, Inc.: 2 (https://510kreport.com/company/fortress-lite-style-wheelchairs)
- Magic-In-Motion, Inc.: 1 (https://510kreport.com/company/magic-in-motion)

## Its most-cited devices
- K990358: Cross Sport, Rigid Wheelchair (1999), cited by 1

## Recent decisions
- K072311: Tilite Aero X (Sep 21, 2007)
- K024055: Tilite Evo (Dec 20, 2002)
- K023606: Tilite YG and Tilite Ygs (Nov 19, 2002)
- K020639: Tipower TR Rimpower and Tipower Tra Rimpower (Jun 20, 2002)
- K020539: Tipower Powerdrive and Rimpower X & SX (Jun 20, 2002)
- K990555: Tisport X and Tisport XC (Mar 22, 1999)
- K990358: Cross Sport, Rigid Wheelchair (Feb 26, 1999)

Source page: https://510kreport.com/company/tisport