510(k) Report

FDA applicant

Liberator Wheelchairs, Inc.

Halton City, TX2 decisions1999–20010 recalls

FDA records 2 decisions for Liberator Wheelchairs, Inc. (Halton City, TX) from 1999 to 2001: 2 510(k) clearances. Most are in product codes ITI (Wheelchair, Powered) and IPL (Wheelchair, Standup). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Liberator Wheelchairs, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Liberator Wheelchairs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Liberator Wheelchairs, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Liberator Wheelchairs, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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