Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007504672

FEI Number

3013473065

Entity Name

CREATIVE DENTAL

City/State/Country

Jinhua City Zhejiang, CN

Establishment Address

No. 99 Ganxi Road, Industrial Park, Jinhua City Zhejiang 321000, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

CREATIVE DENTAL (Owner Number: 10041136)

Owner / Operator Contact Address

No. 99 Ganxi Road, Industrial Park, Jinhua City, CN-ZJ 321000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Tube Band Wires Plier

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DZD	Tube, Orthodontic	Dental	Class 1	872.5410	2012-06-24
ECM	Band, Preformed, Orthodontic	Dental	Class 1	872.5410	2012-06-24
DZC	Wire, Orthodontic	Dental	Class 1	872.5410	2012-06-24
JEX	Plier, Orthodontic	Dental	Class 1	872.4565	2012-06-24

Official Correspondent

XIAOHAN XU

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

CREATIVE DENTAL

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K112640	Ormco Corp.	HYPERELASTIC WIRE	2011-11-16

Similar Registrations

Registration Number	Establishment Name	Location
3006707038	MYOFUNCTIONAL RESEARCH CORP. PTY. LTD.	HELENSVALE Queensland, AU
3032027578	Solventum Orthodontics Corporation	Monrovia, CA, US
1526352	SUMMIT ORTHODONTIC SERVICES, INC.	Schaumburg, IL, US
3014425175	Sharp Detail Orthodontic Laboratory S DE EL DE CV	Tijuana Baja California, MX
3015337428	GUANGZHOU CHEER-U MATERIAL TECHNOLOGY CO., LTD	Guangzhou Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007504672. Last updated year: 2026. Please use registration number 3007504672 when referencing this establishment in official correspondence.