510(k) Report

FDA applicant

Mechanical Application Designs, Inc.

Katy, TX3 decisions1996–19970 recalls

FDA records 3 decisions for Mechanical Application Designs, Inc. (Katy, TX) from 1996 to 1997: 3 510(k) clearances. 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 Mechanical Application Designs, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mechanical Application Designs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mechanical Application Designs, 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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