FDA applicant

Major Mobility Products, Inc.

Houston, TX4 decisions1999–20020 recalls

FDA records 4 decisions for Major Mobility Products, Inc. (Houston, TX) from 1999 to 2002: 4 510(k) clearances. All are in product code IOR (Wheelchair, Mechanical). 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 Major Mobility Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Major Mobility Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Major Mobility Products, 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 “Major”

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

Major Prodotti Dentari S.P.A. 3

Major Mobility Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Major”