Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017178493

FEI Number

3017178493

Entity Name

DONGGUAN CITY SINOSHINE TECHNOLOGY CO.,LTD

City/State/Country

Dongguan Guangdong, CN

Establishment Address

No 488 Jinlang South Road, Shabu Village, Dalang Town, Dongguan Guangdong 523791, CN

Establishment Type(s)

Manufacture Medical Device,Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

DONGGUAN CITY SINOSHINE TECHNOLOGY CO.,LTD (Owner Number: 10075121)

Owner / Operator Contact Address

No 488 Jinlang South Road, Shabu Village, Dalang Town, Dongguan, CN-GD 523791, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Portable Nebulizer GW008, GW008 GWM-01A; GWM-01B; GWM-01C; nebulizer; sshine Manus Nebulizer P601, RX050X-02, RX050X-03 MANUAL INHALER SPACER P601

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CCQ	Nebulizer, Medicinal, Non-Ventilatory (Atomizer)	Anesthesiology	Class 1	868.5640	2025-08-22
EPN	Pump, Nebulizer, Manual	Ear, Nose, Throat	Class 1	874.5220	2020-06-07

Official Correspondent

Joan Chen

US Agent Details

Haiyan Deng Business: UGK-L Technology Service Email: hery-ser@outlook.com Phone: (805) 3513025

Related Public Records

Same Entity

DONGGUAN CITY SINOSHINE 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 3017178493. Last updated year: 2026. Please use registration number 3017178493 when referencing this establishment in official correspondence.