SEKI AOI TECHNO.CO.,LTD

FDA Device Registration & Listing · Nukata-gun Aichi, JP · Registration 3017845230

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
3017845230
FEI Number
3017845230
Entity Name
SEKI AOI TECHNO.CO.,LTD
City/State/Country
Nukata-gun Aichi, JP
Establishment Address
Nukata-gun, Nukata-gun Aichi 4440102, JP
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
SEKI AOI TECHNO.CO.,LTD (Owner Number: 10079256)
Owner / Operator Contact Address
4-27-6, Hachiouji-shi?Koyasu-cho, JP-13 1920904, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOX Chart, Visual Acuity Ophthalmic Class 1 886.1150 2020-11-25

Official Correspondent

Masaaki Urano

US Agent Details

Koji Torii Business: NIDEK INCORPORATED Email: koji_torii@nidek.com Phone: (800) 2239044

Related Public Records

Same Entity

SEKI AOI TECHNO.CO.,LTD
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017845230. Last updated year: 2026. Please use registration number 3017845230 when referencing this establishment in official correspondence.
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