RIGHT MFG. CO., LTD.

FDA Device Registration & Listing · Itabashi-Ku Tokyo, JP · Registration 3004438257

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
3004438257
FEI Number
3004438257
Entity Name
RIGHT MFG. CO., LTD.
City/State/Country
Itabashi-Ku Tokyo, JP
Establishment Address
1-47-3, Maenocho, Itabashi-Ku Tokyo 174-8633, JP
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
RIGHT MFG. CO., LTD. (Owner Number: 10036062)
Owner / Operator Contact Address
1-47-3, Maenocho, Itabashi-ku, JP-13 174-8633, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

LED Slit Lamp MW50D Hand Held Auto Refractometer Retinomax 5 Hand Held Auto Refract-Keratometer Retinomax K-plus5 Auto Refract-Keratometer Speedy-K2 Hand Held Auto Refractometer Retinomax Screeen Hand Held Auto Refract-Keratometer Retinomax K+Screeen

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HJO Biomicroscope, Slit-Lamp, Ac-Powered Ophthalmic Class 2 886.1850 2014-06-20
HKO Refractometer, Ophthalmic Ophthalmic Class 1 886.1760 2011-04-18

Official Correspondent

Yasukatsu Oyama

US Agent Details

Peter G. Sparacio Business: Visionix USA Inc. Email: p.sparacio@visionix.com Phone: (630) 5090949

Related Public Records

Same Entity

RIGHT MFG. 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 3004438257. Last updated year: 2026. Please use registration number 3004438257 when referencing this establishment in official correspondence.
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