Company ยท US
Tisport
FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2007. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
3recalls (0 in 12 months)
3recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 21, 2007 | K072311 | TILITE AERO X Tisport, LLC | IOR |
| Dec 20, 2002 | K024055 | TILITE EVO Tisport, LLC | IOR |
| Nov 19, 2002 | K023606 | TILITE YG AND TILITE YGS Tisport | IOR |
| Jun 20, 2002 | K020639 | TIPOWER TR RIMPOWER AND TIPOWER TRA RIMPOWER Tisport | ITI |
| Jun 20, 2002 | K020539 | TIPOWER POWERDRIVE AND RIMPOWER X & SX Tisport | ITI |
| Mar 22, 1999 | K990555 | TISPORT X AND TISPORT XC Tisport | IOR |
| Feb 26, 1999 | K990358 | CROSS SPORT, RIGID WHEELCHAIR Tisport | IOR |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 24, 2021 | TiSport, Llc Permobil TiLite, Models: Aero Z, and ZRA Open, Classified |
IOR | K990358 |
| Sep 11, 2018 | TiSport, Llc 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-tip extension for manual wheelchairs).
Product Usage:
The Terminated |
IOR | K023606 K072311 +1 |
| Sep 7, 2011 | TiSport, Llc TiLite ZR and ZRA Series 2 are mechanical wheelchairs. Devices are sold under brand name TiLite.
The TiLite ZR had a model catalog number of Z2FS1.
The TiLite ZRA has a model catalog number of Z2F Terminated |
IOR | K990358 |