Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012460677

FEI Number

3012460677

Entity Name

KANEMATSU CHEMICALS CORPORATION

City/State/Country

Tokyo, JP

Establishment Address

8-1, Nihonbashi-Ningyo-cho,, 3-Chome, Chuo-ku, Tokyo 1030013, JP

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Kanematsu Chemicals Corporation (Owner Number: 10050787)

Owner / Operator Contact Address

8-1, Nihonbashi-Ningyo-cho,, 3-Chome, Chuo-ku, Tokyo, JP-13 1030013, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NUQ	Pad, Menstrual, Reusable	Obstetrics/Gynecology	Class 1	884.5435	2015-12-27
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2015-12-27

Official Correspondent

Yumiko Yamauchi

US Agent Details

Yusuke Okada Business: Pacific Marketing Alliance, Inc. Email: okada@pmaiusa.com Phone: (310) 6617260

Related Public Records

Same Entity

Kanematsu Chemicals Corporation

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012460677. Last updated year: 2026. Please use registration number 3012460677 when referencing this establishment in official correspondence.