H. OGINO & CO., LTD.

FDA Device Registration & Listing · Yokohama Kanagawa, JP · Registration 5470

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
5470
FEI Number
5470
Entity Name
H. OGINO & CO., LTD.
City/State/Country
Yokohama Kanagawa, JP
Establishment Address
Yamashitacho 75, Nakaku, Yokohama Kanagawa 2310023, JP
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
H. Ogino & Co., Ltd. (Owner Number: 10051654)
Owner / Operator Contact Address
Yamashitacho 75, Nakaku, Yokohama, JP-14 2310023, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Set, lens, trial, ophthalmic Refractor, manual, non-powered, including phoropter Frame, trial, ophthalmic Exophthalmometer Chart, visual acuity

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HPC Set, Lens, Trial, Ophthalmic Ophthalmic Class 1 886.1405 2016-04-17
HKN Refractor, Manual, Non-Powered, Including Phoropter Ophthalmic Class 1 886.1770 2016-04-17
HPA Frame, Trial, Ophthalmic Ophthalmic Class 1 886.1415 2016-04-17
HLS Exophthalmometer Ophthalmic Class 1 886.1270 2016-04-17
HOX Chart, Visual Acuity Ophthalmic Class 1 886.1150 2016-04-17

Official Correspondent

Shota Nakagawa

US Agent Details

Cheryl Bennett Business: Marco Ophthalmic, Inc. Email: cbennett@marco.com Phone: (904) 6429330

Related Public Records

Same Entity

H. Ogino & Co., Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K900478 Woodlyn, Inc. WOODLYN FULL APERTURE TRIAL LENS SET 1990-02-21

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 5470. Last updated year: 2026. Please use registration number 5470 when referencing this establishment in official correspondence.
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