Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004402508

FEI Number

3004402508

Entity Name

METROPOLITAN GRAPHIC ARTS, INC.

City/State/Country

Gurnee, IL, US

Establishment Address

3818 Grandville Ave, Gurnee, IL 60031, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Metropolitan Graphic Arts, Inc. (Owner Number: 9099541)

Owner / Operator Contact Address

3818 Grandville, Gurnee, IL 60031, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K062602

PMA Number

N/A

All Registered Proprietary Names

Bandage, Liquid UNSCENTED PAD MENSTRUAL U by Kotex, Kotex Pad, Menstrual, Unscented Bandage, Liquid GARMENT FOR INCONTINENCE Garment, Protective, for Incontinence MENSTRUAL Pads, Menstrual, Scented, Deoderized PADS SCENTED-DEODORIZED One By Poise, U by Kotex, Depend, Kotex Bandage, Liquid

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KMF	Bandage, Liquid	General Hospital	Class 1	880.5090	2010-03-29
HHD	Pad, Menstrual, Unscented	Obstetrics/Gynecology	Class 1	884.5435	2007-03-26
KMF	Bandage, Liquid	General Hospital	Class 1	880.5090	2010-03-29
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2007-03-26
NRC	Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile	Obstetrics/Gynecology	Class 1	884.5425	2007-03-26
KMF	Bandage, Liquid	General Hospital	Class 1	880.5090	2010-03-29

Official Correspondent

Mizraim Ramos

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Metropolitan Graphic Arts, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K823241	Kimberly-Clark Corp.	NEW FREEDOM THIN UNSCENTED MAXI PADS	1982-12-28

Similar Registrations

Registration Number	Establishment Name	Location
1628114	DPT LABORATORIES, LTD.	SAN ANTONIO, TX, US
1058584	Sterigenics US LLC	Charlotte, NC, US
2029275	Sterigenics U.S., LLC	Corona, CA, US
3005139112	PERSTORP SPECIALTY CHEMICALS AB, PERSTORP PHARMA	PERSTORP Skane lan [SE-12], SE
3031757047	Solventum US LLC	Brookings, SD, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004402508. Last updated year: 2026. Please use registration number 3004402508 when referencing this establishment in official correspondence.