510(k) Report

FDA applicant

S.C. Johnson & Son, Inc.

Racine, WI5 decisions1982–19960 recalls

FDA records 5 decisions for S.C. Johnson & Son, Inc. (Racine, WI) from 1982 to 1996: 5 510(k) clearances. Most are in product codes LRJ (Disinfectant, Medical Devices) and IMD (Pack, Hot Or Cold, Disposable). 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 S.C. Johnson & Son, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for S.C. Johnson & Son, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — S.C. Johnson & Son, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like S.C. Johnson & Son, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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