FDA applicant

Allergy Laboratories of Ohio, Inc.

Columbus, OH1 decision1987–19870 recalls

FDA records 1 decision for Allergy Laboratories of Ohio, Inc. (Columbus, OH) in 1987: 1 510(k) clearance. All are in product code FMI (Needle, Hypodermic, Single Lumen). 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 Laboratories of Ohio, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Allergy Laboratories of Ohio, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Allergy Laboratories of Ohio, 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 “Allergy”

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

Allergy Extract Co. 1 Allergy Direct 1 Allergy Control Products, Inc. 1 Allergy & Applicator Depot, LLC 1

Allergy Laboratories of Ohio, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Allergy”