IIDA HOSIERY CO.,LTD.

FDA Device Registration & Listing · KISHIMA Saga, JP · Registration 3010897276

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
3010897276
FEI Number
3010897276
Entity Name
IIDA HOSIERY CO.,LTD.
City/State/Country
KISHIMA Saga, JP
Establishment Address
1619,YAMAGUCHI,KOHOKU, KISHIMA Saga 8490501, JP
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Remanufacture Medical Device,Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
IIDA HOSIERY CO.,LTD (Owner Number: 10046637)
Owner / Operator Contact Address
1619,yamaguchi,kohoku,, kishima, JP-41 8490501, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

VANTELIN SUPPORT

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FQL Stocking, Medical Support (For General Medical Purposes) General Hospital Class 1 880.5780 2014-04-20

Official Correspondent

TAKUJI IIDA

US Agent Details

Tetsuya Hiroyama Email: thiroyama@kowa.com Phone: (617) 7920271

Related Public Records

Same Entity

IIDA HOSIERY CO.,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 3010897276. Last updated year: 2026. Please use registration number 3010897276 when referencing this establishment in official correspondence.
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