Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014593130

FEI Number

3014593130

Entity Name

Dongguan Liangyou Electronic Technology Co. Ltd.

City/State/Country

DongGuan Guangdong, CN

Establishment Address

No. 76, 13 Longyan Road, longyan Industrie Area, DongGuan Guangdong 523920, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Revpart (Owner Number: 10094340)

Owner / Operator Contact Address

129 Bethea Road, Suite 402, Fayetteville, GA 30214, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Venturi Vortex Valve Cleaner Venturi Endoscope Channel Cleaning Device Venturi Endoscope Channel Drying Device Venturi MicroDryer Filtered Air Tubing Set

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MNL	Accessories, Cleaning Brushes, For Endoscope	Gastroenterology, Urology	Class 1	876.1500	2025-11-24

Official Correspondent

Sang Lau

US Agent Details

Sang Lau Email: sang@revpart.com Phone: (404) 9912288

Related Public Records

Same Entity

Revpart

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 3014593130. Last updated year: 2026. Please use registration number 3014593130 when referencing this establishment in official correspondence.