510(k) Report

FDA applicant

Mobility Mfg. Co.

Tucson, AZ3 decisions1992–19920 recalls

FDA records 3 decisions for Mobility Mfg. Co. (Tucson, AZ) in 1992: 3 510(k) clearances. All are in product code INI (Vehicle, Motorized 3-Wheeled). 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 Mobility Mfg. Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mobility Mfg. Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Mobility”

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