Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list TiSport with 7 510(k) clearances and 2 device recalls. The most recent is a device recall dated Sep 24, 2021: Permobil TiLite, Models: Aero Z, and ZRA.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Sep 24, 2021 | Permobil TiLite, Models: Aero Z, and ZRAClass II · Some affected wheelchairs, with transit tie downs, that are used as a passenger seat in a motor vehicle may not be confi | Device recalls |
| Sep 11, 2018 | TiLite X-Short anti-tip tubes, models TRA, AERO T, ZRA, AERO Z, 2GX, AERO X, Twist, and AERO R, a component of the TiLite wheelchair (anti-tClass II · The anti-tip tubes potentially fail in certain situations and the wheelchairs can tip backwards. | Device recalls |
| Sep 21, 2007 | TILITE AERO XK072311 · IOR | 510(k) clearances |
| Dec 20, 2002 | TILITE EVOK024055 · IOR | 510(k) clearances |
| Nov 19, 2002 | TILITE YG AND TILITE YGSK023606 · IOR | 510(k) clearances |
| Jun 20, 2002 | TIPOWER TR RIMPOWER AND TIPOWER TRA RIMPOWERK020639 · ITI | 510(k) clearances |
| Jun 20, 2002 | TIPOWER POWERDRIVE AND RIMPOWER X & SXK020539 · ITI | 510(k) clearances |
| Mar 22, 1999 | TISPORT X AND TISPORT XCK990555 · IOR | 510(k) clearances |
| Feb 26, 1999 | CROSS SPORT, RIGID WHEELCHAIRK990358 · IOR | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
