Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3044905064

FEI Number

3044905064

Entity Name

GUANGDONG YOUHONG MEDICAL TECHNOLOGY CO., LTD

City/State/Country

Dongguan Guangdong, CN

Establishment Address

Room 902, Building 6, No. 4 Information Road, Songshanhu District, Dongguan Guangdong 523787, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Guangdong Youhong Medical Technology Co., Ltd (Owner Number: 10095403)

Owner / Operator Contact Address

Unit 2, Building 4, No. 3 Nanshan Road, Songshanhu District, Dongguan, CN-GD 523799, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

V5, V8 Wearable Pulse Oximeter, Model X3, Specification: 7#,8#,9#,10#,11#,12#,13#,14# Mimo Pod

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PGJ	Oximeter, Wellness	Cardiovascular	Class 2	870.2700	2026-03-09
ION	Exerciser, Non-Measuring	Physical Medicine	Class 1	890.5370	2026-04-22

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

Guangdong Youhong Medical 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 3044905064. Last updated year: 2026. Please use registration number 3044905064 when referencing this establishment in official correspondence.