510(k) Report

FDA applicant

Allergy Extract Co.

Hilliard, OH1 decision1993–19930 recalls

FDA records 1 decision for Allergy Extract Co. (Hilliard, OH) in 1993: 1 510(k) clearance. All are in product code SCL (Allergen And Vaccine Delivery Needles). 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 Extract Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Allergy Extract Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Allergy Extract Co. 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.