Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003587170

FEI Number

3003587170

Entity Name

NITTO DENKO CORP.

City/State/Country

OHSAKI CITY Miyagi, JP

Establishment Address

101, SUNADA, SHIMONOME IWADEYAMA, OHSAKI CITY Miyagi 989-6493, JP

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

NITTO DENKO CORP. (Owner Number: 9048993)

Owner / Operator Contact Address

1-1-2, SHIMOHOZUMI, --, IBARAKI CITY, JP-27 5678680, JP

Initial Importer Flag

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
FQM	Bandage, Elastic	General Hospital	Class 1	880.5075	2008-12-04

Official Correspondent

No official correspondent registered.

US Agent Details

Susan Qu Business: NITTO DENKO Avecia Inc. Email: susan.qu@nitto.com Phone: (857) 3786341

Related Public Records

Same Entity

NITTO DENKO CORP.

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 3003587170. Last updated year: 2026. Please use registration number 3003587170 when referencing this establishment in official correspondence.