Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006629593

FEI Number

3006629593

Entity Name

RYOHIN KEIKAKU CO., LTD.

City/State/Country

Bunkyo-ku Tokyo, JP

Establishment Address

2-5-1, Koraku, Sumitomo Fudosan Iidabashi First Bldg, Bunkyo-ku Tokyo 112-0004, JP

Establishment Type(s)

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

Owner / Operator

MUJI U.S.A. LIMITED (Owner Number: 9098161)

Owner / Operator Contact Address

250 WEST 39TH STREET,STE 203, --, New York, NY 10018, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MUJI

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KXG	Applicator, Absorbent Tipped, Sterile	General Hospital	Class 1	880.6025	2007-05-01

Official Correspondent

Yuka Sakamoto

US Agent Details

Yuka Sakamoto Business: MUJI U.S.A. LIMITED Email: HH.IMPORT@MUJI.COM Phone: (646) 3660515

Related Public Records

Same Entity

MUJI U.S.A. LIMITED

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 3006629593. Last updated year: 2026. Please use registration number 3006629593 when referencing this establishment in official correspondence.