FDA applicant
Tampax, Inc.
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
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.
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.
See the 510(k) Report