510(k) Report

FDA applicant

Max Mobility, LLC

Antioch, TN3 decisions2010–20157 recalls

FDA records 3 decisions for Max Mobility, LLC (Antioch, TN) from 2010 to 2015: 3 510(k) clearances. Most are in product codes ITI (Wheelchair, Powered) and IPL (Wheelchair, Standup). 7 recalls are linked to its devices, 5 Class I.

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 Max Mobility, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2010: 12012: 12015: 1
2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

3in 2025

2023: 22024: 2, 2 Class I2025: 3, 3 Class I
2010high 3 (2025) · low 0 (2010)2026

Class I Class II/III not classified

FIG. 1 — Max Mobility, LLC by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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