Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008542991

FEI Number

3008542991

Entity Name

TAISEI KAKO CO., LTD.

City/State/Country

Ibaraki Osaka, JP

Establishment Address

Ibaraki Factory, Fujinosato 2-11-6, Ibaraki Osaka 567-0054, JP

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Taisei Kako Co., Ltd. (Owner Number: 10061202)

Owner / Operator Contact Address

Fujinosato 2-11-6, Ibaraki, JP-27 567-0054, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Syringe Adapter

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GCD	Connector, Catheter	General, Plastic Surgery	Class 1	878.4200	2025-06-11

Official Correspondent

Keiko Ishii

US Agent Details

Alan Miskewicz Business: 3D-Matrix Email: amiskewicz@3dmatrix.com Phone: (781) 3739020

Related Public Records

Same Entity

Taisei Kako 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 3008542991. Last updated year: 2026. Please use registration number 3008542991 when referencing this establishment in official correspondence.