Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8030433

FEI Number

3009662620

Entity Name

ATAGO CO., LTD.

City/State/Country

Minato-ku Tokyo, JP

Establishment Address

2-6-3 Shiba-koen, The Front Tower Shiba Koen 23rd Floor, Minato-ku Tokyo --, JP

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ATAGO CO., LTD. (Owner Number: 8030433)

Owner / Operator Contact Address

2-6-3 Shiba-koen, The Front Tower Shiba Koen 23rd Floor, Minato-ku, TOKYO, JP-NOTA --, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ATAGO

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HKO	Refractometer, Ophthalmic	Ophthalmic	Class 1	886.1760	2005-03-03

Official Correspondent

No official correspondent registered.

US Agent Details

Yusuke Amamiya Business: ATAGO U.S.A., Inc Email: yusuke@atago-usa.com Phone: (425) 6372107

Related Public Records

Same Entity

ATAGO 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 8030433. Last updated year: 2026. Please use registration number 8030433 when referencing this establishment in official correspondence.