# K072311: Tilite Aero X

- Pathway: 510(k) (Abbreviated)
- Applicant: Tisport, LLC
- Decided: Sep 21, 2007 after 35 days
- Product code: IOR (Wheelchair, Mechanical)
- Device class: 1
- Regulation: 21 CFR 890.3850
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K890050 (1989). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K890050: Zippie & Quickie 2HP Wheelchair, Motion Designs, Inc. (1989) Summary page 1.

## Recalls of this device
- Sep 11, 2018 · Class II · Z-2294-2019: The anti-tip tubes potentially fail in certain situations and the wheelchairs can tip backwards.

## Indications for use
The intended use for the TiLite Aero X is to provide mobility to physically impaired individuals.

Source page: https://510kreport.com/device/K072311
Methodology: https://510kreport.com/methodology