Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3038209294

FEI Number

3038209294

Entity Name

DONGGUAN YIYAO SCIENCE & TECHNOLOGY DEVELOPMENT CO., LTD.

City/State/Country

Dongguan City Guangdong, CN

Establishment Address

Room501, NO. 11 Shennan yiheng street, Shenxiang, Qishi Town, Dongguan City Guangdong 523000, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Dongguan Yiyao Science & Technology Development Co., Ltd. (Owner Number: 10093234)

Owner / Operator Contact Address

Room501, NO. 11 Shennan yiheng street, Shenxiang, Qishi Town, Dongguan City, CN-GD 523000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Anti Snore Mouthpiece, Device, Anti-Snoring-BreazTek Anti Snore Mouthpiece, Kaitse ANTI SNORE MOUTHPIECE orthodont dental, dental orthodont, orthodontic tools dental Orthodontics, Dental Orthodontic Brackets, Dental Orthodontics, Dental Orthodontic Retainer instruments, Dental Orthodontic Retainer instruments (Positioner, Tooth, Preformed, Preformed tooth positione, Braces Orthodont,

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2025-12-01
KMY	Positioner, Tooth, Preformed	Dental	Class 1	872.5525	2025-04-16

Official Correspondent

Xianzhao Tang

US Agent Details

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

Related Public Records

Same Entity

Dongguan Yiyao Science & Technology Development Co., Ltd.

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
K122391	Medtronic Xomed, Inc.	MEDTRONIC XOMED, INC.	2013-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038209294. Last updated year: 2026. Please use registration number 3038209294 when referencing this establishment in official correspondence.