510(k) Report

FDA applicant

Vector Mobility, Inc.

Fresno, CA2 decisions1994–19940 recalls

FDA records 2 decisions for Vector Mobility, Inc. (Fresno, CA) in 1994: 2 510(k) clearances. Most are in product codes IOR (Wheelchair, Mechanical) 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 Vector Mobility, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vector Mobility, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Vector Mobility, 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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Other applicant names beginning “Vector”

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