Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014795329

FEI Number

3014795329

Entity Name

GUANGZHOU MINGYAN BIOTECHNOLOGY CO.,LTD

City/State/Country

Guangzhou Guangdong, CN

Establishment Address

No.1 Meiyan Avenue, Yingchun Road, Huadu District, Guangzhou Guangdong 510810, CN

Establishment Type(s)

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

Owner / Operator

Guangzhou Mingyan Biotechnology Co.,Ltd (Owner Number: 10088099)

Owner / Operator Contact Address

No.1 Meiyan Avenue, Yingchun Road, Huadu District, Guangzhou, CN-GD 510810, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Acne pacth Scar gel, Scar dressing Sheet, Scar Tape/Rope, Scar cream

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NAC	Dressing, Wound, Hydrophilic	General, Plastic Surgery	Class 1	878.4018	2023-05-24
MDA	Elastomer, Silicone, For Scar Management	General, Plastic Surgery	Class 1	878.4025	2023-05-24

Official Correspondent

Emma Liang

US Agent Details

Aokai Tang Business: AOKT STUDIO LLC Email: aokt-service@outlook.com Phone: (757) 2240177

Related Public Records

Same Entity

Guangzhou Mingyan Biotechnology Co.,Ltd

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3027643662	ERIBIOTECH CO.,LTD	Suzhou Jiangsu, CN
3006607005	MOLNLYCKE HEALTH CARE (THAILAND), LTD.	Amphur Muang Chonburi Chon Buri, TH
3015432652	E.L.F. COSMETICS INC	Oakland, CA, US
3043138901	DONGGUAN SAMVO BIOTECHNOLOGY CO., LTD	Dongguan Guangdong, CN
3015215566	THE HAIN CELESTIAL GROUP	Hoboken, NJ, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014795329. Last updated year: 2026. Please use registration number 3014795329 when referencing this establishment in official correspondence.