Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010579827

FEI Number

3010579827

Entity Name

YAMAMOTO CORPORATION

City/State/Country

Osaka, JP

Establishment Address

5-13-11,nakagawa,ikuno-ku, Osaka 544-0005, JP

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Yamamoto Corporation (Owner Number: 10045241)

Owner / Operator Contact Address

5-13-11,nakagawa,ikuno-ku, Osaka, JP-27 544-0005, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

"Yamamoto" Biorubber AERODOME Far Infrared Belt (Non-sterile) "Yamamoto" Biorubber AERODOME Far Infrared Truncal Protector (Non-sterile) "Yamamoto" Biorubber AERODOME Far Infrared Supporter(Non-sterile)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MRI	Orthosis, Truncal/Orthosis, Limb	Physical Medicine	Class 1	890.3490	2013-10-30
ITM	Cage, Knee	Physical Medicine	Class 1	890.3475	2014-04-25

Official Correspondent

Tomizo Yamamoto

US Agent Details

Akikazu Kimura Business: AKT Trading Inc. Email: info@aktusa.com Phone: (310) 7152174

Related Public Records

Same Entity

Yamamoto 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 3010579827. Last updated year: 2026. Please use registration number 3010579827 when referencing this establishment in official correspondence.