FDA applicant

Huntington Laboratories, Inc.

Huntington, IN7 decisions1985–19960 recalls

FDA records 7 decisions for Huntington Laboratories, Inc. (Huntington, IN) from 1985 to 1996: 7 510(k) clearances. Most are in product codes LRJ (Disinfectant, Medical Devices) and KMJ (Lubricant, Patient). 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 Huntington Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Huntington Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Huntington Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?