KANEHARA TRADING, INC./ KANEHARA

FDA Device Registration & Listing · Yushima, Bunkyo-ku Tokyo, JP · Registration 3009450901

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009450901
FEI Number
3009450901
Entity Name
KANEHARA TRADING, INC./ KANEHARA
City/State/Country
Yushima, Bunkyo-ku Tokyo, JP
Establishment Address
31-14, 2-chome, Yushima, Bunkyo-ku Tokyo 113-0034, JP
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Kanehara Trading, Inc./ Kanehara (Owner Number: 10040310)
Owner / Operator Contact Address
31-14, 2-chome, Yushima, Bunkyo-ku, JP-13 113-0034, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Ishihara

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HIT Tester, Color Vision Ophthalmic Class 1 886.1170 2012-03-30

Official Correspondent

No official correspondent registered.

US Agent Details

Amy Piccini Business: GF Health Products, Inc. Email: apiccini@grahamfield.com Phone: (678) 2913282

Related Public Records

Same Entity

Kanehara Trading, Inc./ Kanehara
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009450901. Last updated year: 2026. Please use registration number 3009450901 when referencing this establishment in official correspondence.
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