510(k) Report

FDA applicant

Amigo Mobility Intl., Inc.

Bridgeport, MI8 decisions1994–20100 recalls

FDA records 8 decisions for Amigo Mobility Intl., Inc. (Bridgeport, MI) from 1994 to 2010: 8 510(k) clearances. Most are in product codes INI (Vehicle, Motorized 3-Wheeled) and 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 Amigo Mobility Intl., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2009: 12010: 1
2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Amigo”

FDA records each applicant name separately; these may or may not be the same firm.