Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027555943

FEI Number

3027555943

Entity Name

GC Corporation Mishima Factory

City/State/Country

Sunto-Gun Shizuoka, JP

Establishment Address

454-1 Higashino, Nagaizumi-Cho, Sunto-Gun Shizuoka 411-0931, JP

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

GC America Inc. (Owner Number: 8030268)

Owner / Operator Contact Address

3737 W. 127th Street, Alsip, IL 60803, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Dupli Coi Loid

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EIS	Remover, Crown	Dental	Class 1	872.4565	2001-04-14

Official Correspondent

Futoshi Fusejima

US Agent Details

Futoshi Fusejima Business: GC America Inc. Email: futoshi.fusejima@gc.dental Phone: (708) 8970900

Related Public Records

Same Entity

GC America Inc.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3004146043	GC ASAHI CORPORATION	AICHI, JP
3001949270	WINNING APPLIANCE MANUFACTORY LIMITED	CHAI WAN HONG KONG Xinjiang, CN
3004046512	TSUEN LEE METALS & PLASTIC TOYS FACTORY	SHEN ZHEN CITY Guangdong, CN
9710611	STICK TECH LTD.	TURKU Pirkanmaa, FI
3003941201	NIMI CHEMICAL INDUSTRIAL CO., LTD.	Kiryu Gunma, JP

Similar Registrations

Registration Number	Establishment Name	Location
9611367	HELMUT ZEPF MEDIZINTECHNIK GMBH	SEITINGEN Baden-Wurttemberg, DE
1215305	PULPDENT CORPORATION	Watertown, MA, US
9610612	AESCULAP AG	TUTTLINGEN, DONAU Baden-Wurttemberg, DE
3010055973	YCH DISTRIPARK SDN BHD	Prai Pulau Pinang, MY
3015422158	ARTCRAFT DENTAL, INC.	Dallas, TX, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027555943. Last updated year: 2026. Please use registration number 3027555943 when referencing this establishment in official correspondence.