Tisport, LLC
Tisport, LLC holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2007, with 2 FDA device recalls on record.
Top product codes for Tisport, LLC
FDA recalls by Tisport, LLC
- Z-0264-2022 — Permobil TiLite, Models: Aero Z, and ZRA
- Z-2294-2019 — 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 affected component is part of a manual wheelchair to provide mobility to physically impaired individuals. The affected component is used to prevent the wheelchair from tipping backwards.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Tisport, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.