Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005619472

FEI Number

3005619472

Entity Name

T.M.I. COMPANY, LIMITED

City/State/Country

NIIZA, Saitama, JP

Establishment Address

2-10, 1-CHROME NIIZA, NIIZA, Saitama --, JP

Establishment Type(s)

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

Owner / Operator

T.M.I. COMPANY, LIMITED (Owner Number: 9083409)

Owner / Operator Contact Address

2-10, NIIZA 1-CHROME, --, NIIZA, SAITAMA, JP-NOTA --, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ISHIHARA'S TEST BOOK

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HIT	Tester, Color Vision	Ophthalmic	Class 1	886.1170	2006-02-24

Official Correspondent

No official correspondent registered.

US Agent Details

Sean Cockley Email: SEAN@GULDENOPHTHALMICS.COM Phone: (215) 8848105

Related Public Records

Same Entity

T.M.I. COMPANY, LIMITED

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

View Entity Profile →

Similar Registrations

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3014274073	WAGGONER COLOR VISION TESTING, LLC.	Bentonville, AR, US
2518410	GULDEN OPHTHALMICS	Elkins Park, PA, US
3016491661	TITMUS LLC	Fulton, MD, US
3017657497	HERU, INC.	Miami, FL, US
3006550126	SPEEDWAY	India Delhi, IN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005619472. Last updated year: 2026. Please use registration number 3005619472 when referencing this establishment in official correspondence.