Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005051467

FEI Number

3005051467

Entity Name

KOKUBO Co., Ltd

City/State/Country

Kainan Wakayama, JP

Establishment Address

201-9, Nokamishin, Kainan Wakayama 6401161, JP

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

KOKUBO Co.,Ltd (Owner Number: 10090161)

Owner / Operator Contact Address

8th Floor, 2-3-6, Nihonbashi, Chuo-ku, JP-13 103-0027, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Foot Patch - Ginseng Foot Patch - Jyueki-Ryoku Foot Patch - Catechin Foot Patch - Mugwort Foot Patch - Tea Tree Foot Patch - Germanium

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OMW	Adhesive Backed Thermal Skin Patches	Physical Medicine	Class 1	890.5710	2024-02-22

Official Correspondent

Mizuho Okubo

US Agent Details

Toshiko Boyd Business: Eureka Global Solutions LLC Email: toshiko@eureka-global.net Phone: (310) 4356358

Related Public Records

Same Entity

KOKUBO Co.,Ltd

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 3005051467. Last updated year: 2026. Please use registration number 3005051467 when referencing this establishment in official correspondence.