FDA applicant

Allergy Direct

Kansas City, MO1 decision1999–19990 recalls

FDA records 1 decision for Allergy Direct (Kansas City, MO) in 1999: 1 510(k) clearance. All are in product code FMW (Cover, Mattress (Medical Purposes)). 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, general hospital panel, where it files most

How often FDA has decided Allergy Direct’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Allergy Direct since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Allergy”

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

Allergy Extract Co. 1 Allergy Control Products, Inc. 1 Allergy Laboratories of Ohio, Inc. 1 Allergy & Applicator Depot, LLC 1

Allergy Direct

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Allergy”