HHDClass I

Pad, Menstrual, Unscented

21 CFR 884.5435 / Obstetrics/Gynecology

HHD is the FDA product code for Pad, Menstrual, Unscented, a class I device type, regulated under 21 CFR 884.5435. FDA's definition for this code reads: "An unscented menstrual pad which is used to absorb menstrual fluid or other vaginal discharge and is made of common cellulosic and synthetic material with an established safety profile". As of 2026-09-10, FDA records hold 136 510(k) clearances under this code, the most recent dated 2007-09-20, and no recalls.

Classification record

Product code: HHD
Device name: Pad, Menstrual, Unscented
FDA definition: An unscented menstrual pad which is used to absorb menstrual fluid or other vaginal discharge and is made of common cellulosic and synthetic material with an established safety profile.
Regulation: 21 CFR 884.5435
Device class: Class I
Review panel: Obstetrics/Gynecology
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 136
Ingested recalls: 0

Clearances, product code HHD

By decision year

136 clearances under product code HHD with a decision year between 1976 and 2007, 1984 the highest year at 15.

Show the numbers

510(k) clearances under FDA product code HHD by decision year
Year	Clearances
1976	2
1977	1
1978	1
1979	2
1980	5
1981	9
1982	11
1983	7
1984	15
1985	12
1986	12
1987	4
1988	6
1989	7
1990	7
1991	2
1992	1
1993	6
1994	10
1995	11
1998	1
2000	1
2001	2
2007	1

Applicants with the most clearances

Product code HHD

Applicants holding the most 510(k) clearances under product code HHD
Applicant	Clearances
Kimberly-Clark Corporation	13
Personal Products Co.	12
Procter & Gamble Mfg. Co.	11
Tambrands Inc.	10
Kao Corp.	8
Paragon Trade Brands, Inc.	8
I.C.D. Industries, Inc.	6
Procter & Gamble Co.	6
Marcal Paper Mills, Inc.	4
Customed, Inc	3

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 301 companies shown, in name order