TOYO RESIN CORPORATION

FDA Device Registration & Listing · FUJI Shizuoka, JP · Registration 3010195489

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
3010195489
FEI Number
3010195489
Entity Name
TOYO RESIN CORPORATION
City/State/Country
FUJI Shizuoka, JP
Establishment Address
2104-1 ATUHARA, FUJI Shizuoka 4190201, JP
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
TOYO RESIN CORPORATION (Owner Number: 10047597)
Owner / Operator Contact Address
2104-1 ATUHARA, FUJI, JP-22 4190201, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BANDAGE, CAST

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITG Bandage, Cast Physical Medicine Class 1 890.3025 2014-10-09

Official Correspondent

Kenta IDE

US Agent Details

Takahiro Haruyama Email: register@globizz.net Phone: (310) 5383860

Related Public Records

Same Entity

TOYO RESIN CORPORATION
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 3010195489. Last updated year: 2026. Please use registration number 3010195489 when referencing this establishment in official correspondence.
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