Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015522136

FEI Number

3015522136

Entity Name

KANTO GOSEI KOGYO CO.,LTD.

City/State/Country

Sumida-ku Tokyo, JP

Establishment Address

2-35-8 Sumida, Sumida-ku Tokyo 131-0031, JP

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

REPROLIFE INC. (Owner Number: 10060630)

Owner / Operator Contact Address

2-5-3-9F Shinjuku, Shinjuku-ku, JP-13 160-0022, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Tissue Storage: 10 Cryotecs (Blue) Tissue Storage: 10 Cryotecs (Green) Tissue Storage: 10 Cryotecs (Yellow) Tissue Storage: 10 Cryotecs (White) Tissue Storage: 10 Cryotecs (Red) Warm Plate-10 Plates Vitri Plate-10 Plates

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQK	Labware, Assisted Reproduction	Obstetrics/Gynecology	Class 2	884.6160	2022-11-14
PUD	Labware, Assisted Reproduction, Exempt	Obstetrics/Gynecology	Class 2	884.6160	2019-06-04

Official Correspondent

Shin Tanaka

US Agent Details

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

Related Public Records

Same Entity

REPROLIFE INC.

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 3015522136. Last updated year: 2026. Please use registration number 3015522136 when referencing this establishment in official correspondence.