Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9616263

FEI Number

3001229191

Entity Name

PHC Corporation

City/State/Country

Ora-gun Gunma, JP

Establishment Address

1-1-1 Sakada, Oizumi-machi, Ora-gun Gunma 370-0596, JP

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

PHC Corporation (Owner Number: 9052268)

Owner / Operator Contact Address

2131-1 MINAMIGATA, TOON, JP-38 791-0395, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MCO-50M MCO-170MP

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PUB	Accessory, Assisted Reproduction, Exempt	Obstetrics/Gynecology	Class 2	884.6120	2017-09-24

Official Correspondent

No official correspondent registered.

US Agent Details

Joe LaPorte Business: PHC Corporation of North America Email: joe.laporte@us.phchd.com Phone: (630) 6948214

Related Public Records

Same Entity

PHC Corporation

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3029973107	PHC Corporation	Tako-machi Katori-gun Chiba, JP
1000134386	PHC Corporation	TOON Ehime, JP
3014353045	PHC Corporation	Chiyoda-ku Tokyo, JP
3004167884	PHC Corporation	MIMA Tokushima, JP

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3009747883	Esco Medical Technologies, UAB	Ramuciai Kauno Apskritis, LT
3007459332	ASTEC CO., Ltd.	Kasuya Fukuoka, JP
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9616263. Last updated year: 2026. Please use registration number 9616263 when referencing this establishment in official correspondence.