Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043572164

FEI Number

3043572164

Entity Name

HUEZ HAUS SEOUL CO., LTD

City/State/Country

Songpa-gu Seoul, KR

Establishment Address

Unit F-9055, 66 Chungmin-ro, Songpa-gu Seoul 05838, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

HUEZ HAUS SEOUL CO., LTD (Owner Number: 10095109)

Owner / Operator Contact Address

Unit F-9055, 66 Chungmin-ro, Songpa-gu, KR-11 05838, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

huez (LARGE-Heavy Flows (10 count)) huez (MEDIUM-Regular Flows (12 count)) huez (MEDIUM-Regular Flows (2 count)) huez (LINERS-Daily Liner (40 count))

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HHD	Pad, Menstrual, Unscented	Obstetrics/Gynecology	Class 1	884.5435	2026-01-26

Official Correspondent

SungChul Kim

US Agent Details

Jung Ryun Ahn Business: KMC USA, Inc Email: kmc.usa@kmcerti.com Phone: (646) 3576058

Related Public Records

Same Entity

HUEZ HAUS SEOUL CO., LTD

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043572164. Last updated year: 2026. Please use registration number 3043572164 when referencing this establishment in official correspondence.