FDA applicant

Assembly Required Dist., Inc.

Commack, NY1 decision1997–19970 recalls

FDA records 1 decision for Assembly Required Dist., Inc. (Commack, NY) in 1997: 1 510(k) clearance. All are in product code IOR (Wheelchair, Mechanical). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Assembly Required Dist., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Assembly Required Dist., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Assembly Required Dist., Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?