510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K890655Substantially Equivalent

New Freedom Thin Deodorant Maxi Pads

Kimberly-Clark Corporation, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K890655 is the FDA 510(k) clearance record for NEW FREEDOM THIN DEODORANT MAXI PADS, a class II device, cleared for Kimberly-Clark Corp. on under FDA product code HHL (Pad, Menstrual, Scented, Scented-Deodorized). FDA's definition for product code HHL reads: "Scented or scented-deodorized menstrual pads used to absorb menstrual or other vaginal discharge, including those intended as intralabial pads or reusable menstrual pads. These are made with materials that do not meet the requirements for...". FDA records list 122 510(k) clearances for Kimberly-Clark Corp., from to . As of , FDA records show no recalls naming K890655.

Clearance record

Decision date
Received
(82 days to decision)
Product code
HHL Pad, Menstrual, Scented, Scented-Deodorized
Regulation
21 CFR 884.5425
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Kimberly-Clark Corp. 1201 Pennsylvania Ave., NW, Washington DC
Third party review
No

Clearances, product code HHL

Trailing 12 months

FDA records hold no clearances under product code HHL in the trailing twelve months.

FDA records show no clearances under product code HHL in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HHL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260