RICOH COMPANY, LTD.

FDA Device Registration & Listing · Kanazawa Ishikawa, JP · Registration 3014137562

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
3014137562
FEI Number
3014137562
Entity Name
RICOH COMPANY, LTD.
City/State/Country
Kanazawa Ishikawa, JP
Establishment Address
2-3, Hokuyo-dai, Kanazawa Ishikawa 920-0177, JP
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Ricoh Company, Ltd. (Owner Number: 10055737)
Owner / Operator Contact Address
2-3, Hokuyo-dai, Kanazawa, JP-17 920-0177, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K210199
PMA Number
N/A

All Registered Proprietary Names

RICOH MEG RICOH MEG

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OLY Magnetoencephalograph Neurology Class 2 882.1400 2017-10-03
OLX Source Localization Software For Electroencephalograph Or Magnetoencephalograph Neurology Class 2 882.1400 2017-10-03
OLY Magnetoencephalograph Neurology Class 2 882.1400 2021-12-14
OLX Source Localization Software For Electroencephalograph Or Magnetoencephalograph Neurology Class 2 882.1400 2021-12-14

Official Correspondent

No official correspondent registered.

US Agent Details

Amy Trongnetrpunya Email: amy.trongnetrpunya@ricoh-usa.com Phone: (562) 2171498

Related Public Records

Same Entity

Ricoh Company, 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 3014137562. Last updated year: 2026. Please use registration number 3014137562 when referencing this establishment in official correspondence.
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