FOSHAN VOHOM TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · Foshan Guangdong, CN · Registration 3010354914

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
3010354914
FEI Number
3010354914
Entity Name
FOSHAN VOHOM TECHNOLOGY CO., LTD.
City/State/Country
Foshan Guangdong, CN
Establishment Address
4/F, 1 ENT. A3 Bldg., Hantian Science and Technology City, No.17, Shenhai Road, Guicheng Town, Nanhai District, Foshan Guangdong 528200, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Foshan Vohom Technology Co., Ltd. (Owner Number: 10044229)
Owner / Operator Contact Address
4/F, 1 ENT. A3 Bldg., Hantian Science and Technology City, No.17, Shenhai Road, Guicheng Town, Nanhai District, Foshan, CN-GD 528200, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Air-Conduction Hearing Aid Air Conduction Hearing Aid

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 2022-11-24
ESD Hearing Aid, Air-Conduction, Prescription Ear, Nose, Throat Class 1 874.3300 2013-05-15

Official Correspondent

No official correspondent registered.

US Agent Details

Shu-Chen Cheng Business: ROC Chinese-European Industrial Research Society Email: ceirs.jen@msa.hinet.net Phone: (614) 5888168

Related Public Records

Same Entity

Foshan Vohom Technology 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

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Registration Number Establishment Name Location
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3022507139 Zhongrui HearJoy Medical Equipment co., Ltd. Shenzhen Guangdong, CN
3027300374 SHENZHEN AKAUDIO CO., LIMITED Shenzhen Guangdong, CN
3033659461 SHENZHEN SOUNDS GOOD TECHNOLOGIES CO., LTD Shenzhen Guangdong, CN
3008460009 Shenzhen Zhongde Audio-Technical Co., Ltd. Shenzhen City Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010354914. Last updated year: 2026. Please use registration number 3010354914 when referencing this establishment in official correspondence.
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