510(k) Report

FDA applicant

Avon Products, Inc.

New York, NY3 decisions1994–19950 recalls

FDA records 3 decisions for Avon Products, Inc. (New York, NY) from 1994 to 1995: 3 510(k) clearances. Most are in product codes HQY (Sunglasses (Non-Prescription Including…) and ILY (Lamp, Infrared, Therapeutic Heating). 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Avon Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Avon Products, 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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