510(k) Report

FDA applicant

Tampax, Inc.

Mchenry, IL12 decisions1978–19830 recalls

FDA records 12 decisions for Tampax, Inc. (Mchenry, IL) from 1978 to 1983: 12 510(k) clearances. Most are in product codes HEB (Tampon, Menstrual, Unscented) and HHD (Pad, Menstrual, Unscented). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Tampax, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Tampax, 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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