Ultra Maxithins Pads

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K871716 ↗

FDA Product Code

HHD

FDA applicant

Tambrands, Inc.

Device Class

Class I

Regulation

21 CFR Part 884.5435

Advisory Committee

Obstetrics/Gynecology

FDA Decision

SESE Substantially Equivalent

• Unscented Menstrual Tampon, Plastic Applicator

  Class II

  FDA 510(k) K962476 Active Cleared 13 Aug 1996

• Tampax Deodorant Tampon, Slender Regular

  Class II

  FDA 510(k) K872260 Active Cleared 10 Jul 1987

• Modified Regular Deodorant Maxithins Pads

  Class II

  FDA 510(k) K862678 Active Cleared 15 Aug 1986

• Tampax Ultrafit Panty Shields - Mofification

  Class I

  FDA 510(k) K891474 Active Cleared 7 Jun 1989

• Slender Regular Tampons

  Class II

  FDA 510(k) K864650 Active Cleared 4 Mar 1987

• Maxithins Body-Shaped Panty Shields

  Class I

  FDA 510(k) K842951 Active Cleared 23 Aug 1984

See all devices from Tambrands Inc. →