510(k) Report

FDA applicant

Method Mobility

Fresno, CA1 decision2023–20230 recalls

FDA records 1 decision for Method Mobility (Fresno, CA) in 2023: 1 510(k) clearance. All are in product code ITI (Wheelchair, Powered). 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 Method Mobility’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2023: 1
2023high 1 (2023) · low 0 (2024)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2023.

FIG. 1 — Method Mobility by year, 2023–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • ITIWheelchair, Powered1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K231032AMP by Method Mobility, AMP Plus (or +) by Method MobilityMethod Mobility · 20231cites it

What has FDA decided for it lately?

  • K231032AMP by Method Mobility, AMP Plus (or +) by Method MobilityMethod Mobility · 2023

The one decision as Method Mobility →