SHENZHEN BYRING HEARING TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · shenzhen Guangdong, CN · Registration 3043149272

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3043149272
FEI Number
3043149272
Entity Name
SHENZHEN BYRING HEARING TECHNOLOGY CO., LTD.
City/State/Country
shenzhen Guangdong, CN
Establishment Address
1510, Block A, Building 4, Huaqiang Creative Industrial Park, 701 Guangwei Road, Biyan Community, Guangming Street, Guangming District, Shenzhen, shenzhen Guangdong 518107, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Shenzhen Byring Hearing Technology Co., Ltd. (Owner Number: 10094847)
Owner / Operator Contact Address
1510, Block A, Building 4, Huaqiang Creative Industrial Park, 701 Guangwei Road, Biyan Community, Guangming Street, Guangming District, Shenzhen, shenzhen, CN-GD 518107, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Behind The Ear Hearing Aid;Model:Fuxi,Elaphodus,Ocarina,Guqin Behind The Ear Hearing Aid;Model:Fuxi,Elaphodus,Ocarina,Guqin

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QUF Hearing Aid, Air-Conduction, Over The Counter Ear, Nose, Throat Class 1 874.3300 2026-01-07
QUG Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter Ear, Nose, Throat Class 2 874.3305 2026-01-07

Official Correspondent

mengzhu Wang

US Agent Details

mark DU Email: markFDA@outlook.com Phone: (303) 3594188

Related Public Records

Same Entity

Shenzhen Byring Hearing Technology Co., Ltd.
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 3043149272. Last updated year: 2026. Please use registration number 3043149272 when referencing this establishment in official correspondence.
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