510(k) Report

FDA applicant

Clairol, Inc.

Mchenry, IL4 decisions1977–19850 recalls

FDA records 4 decisions for Clairol, Inc. (Mchenry, IL) from 1977 to 1985: 4 510(k) clearances. Most are in product codes IRT (Pad, Heating, Powered) and EFT (Cleanser, Denture, Over The Counter). 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Clairol, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Clairol, 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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