Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004649480

FEI Number

3004649480

Entity Name

ALCARE CO., LTD CHIBA FACTORY, EAST

City/State/Country

CHIBA CITY, JP

Establishment Address

289-4, CHIGUSA-CHO, HANAMIGAWA-KU, CHIBA CITY 262-0012, JP

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

ALCARE CO., LTD (Owner Number: 9003129)

Owner / Operator Contact Address

19F ARCA CENTRAL BLDG., 1-2-1 KINSHI SUMIDA-KU, TOKYO, JP-NOTA 130-0013, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MOLDCARE RI II

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KXH	Cradle, Patient, Radiologic	Radiology	Class 1	892.1830	2004-07-29

Official Correspondent

No official correspondent registered.

US Agent Details

DENO ZACHARY Business: MIC International Email: dzachary@micinternational.com Phone: (917) 3315789

Related Public Records

Same Entity

ALCARE 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 3004649480. Last updated year: 2026. Please use registration number 3004649480 when referencing this establishment in official correspondence.