FDA Device Registration & Listing · Itabashi-Ku Tokyo, JP · Registration 3004438257
Public RecordDevice ListingExpiry 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 MW50DHand Held Auto Refractometer Retinomax 5Hand Held Auto Refract-Keratometer Retinomax K-plus5Auto Refract-Keratometer Speedy-K2Hand Held Auto Refractometer Retinomax ScreeenHand Held Auto Refract-Keratometer Retinomax K+Screeen
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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