SHENZHEN SHENRUI MEDICAL CO. LTD

FDA Device Registration & Listing · Shenzhen Guangdong, CN · Registration 3015763534

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
3015763534
FEI Number
3015763534
Entity Name
SHENZHEN SHENRUI MEDICAL CO. LTD
City/State/Country
Shenzhen Guangdong, CN
Establishment Address
Floor 4, Building C, Fuyongli Xinhu Funing High-tech Industrial Park, Fuyong Street, Baoan District, Shenzhen Guangdong 518103, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Shenzhen Shenrui Medical Co. LTD (Owner Number: 10061027)
Owner / Operator Contact Address
Floor 4, building C, Fuyongli Xinhu Funing High-tech Industrial Park, Fuyong Street, Baoan District, Shenzhen, CN-GD 518103, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

E-216, E-516, E-616, E-632, E-732 Hearing Aid C-109A, C-109B, C-109F D-207, D-501C, D-502C A-22, A-25, A-26, A-27, A-28, A-31, A-32, A-301, A-305 Hearing Aid D-207, D -218, D-502B C-06, C-108, C-109, C-109H, C-109K, C-122 E-206, E-216, E-316

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ESD Hearing Aid, Air-Conduction, Prescription Ear, Nose, Throat Class 1 874.3300 2019-07-31
QUF Hearing Aid, Air-Conduction, Over The Counter Ear, Nose, Throat Class 1 874.3300 2023-11-13

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Mack Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

Shenzhen Shenrui Medical 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
K892457 Telstar Electronics, Inc. TELSTAR MODEL 1/3 ITE HEARING AID 1989-06-06
K760996 Unitron Industries, Inc. HEARING AID (MODEL 695D, 905 & 960P) 1976-11-16
K840825 Maico Hearing Instruments, Inc. SERIES MR IN-THE-EAR CUSTOM HEARING AID 1984-03-30
K946253 Maico Hearing Instruments, Inc. MAICO IN-THE-EAR MODEL RD 201 1995-01-30
K863975 Gn Danavox, Inc. CUSTOM IN-THE-EAR 1986-11-07

Similar Registrations

Registration Number Establishment Name Location
3008713760 KENYON AUDIOLOGY Bend, OR, US
3022507139 Zhongrui HearJoy Medical Equipment co., Ltd. Shenzhen Guangdong, CN
3005785669 ALPS INTERNATIONAL NEW DELHI, IN
2523819 MICROSONIC, INC. AMBRIDGE, PA, US
3017618900 HUIZHOU GOLD ROSE TECHNOLOGY CO.,LTD huizhou Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015763534. Last updated year: 2026. Please use registration number 3015763534 when referencing this establishment in official correspondence.
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