DuoGreen Co., Ltd

FDA Device Registration & Listing · Gangseo-gu Seoul, KR · Registration 3013318814

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
3013318814
FEI Number
3013318814
Entity Name
DuoGreen Co., Ltd
City/State/Country
Gangseo-gu Seoul, KR
Establishment Address
1214-1216, 20, Magokjungang 5-ro 1-gil, Gangseo-gu Seoul 07788, KR
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Duogreen Inc. (Owner Number: 10060228)
Owner / Operator Contact Address
2460 lemoine Ave 302, Unit 2, Fort Lee, NJ 07024, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

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 2019-07-09

Official Correspondent

JAMES OH

US Agent Details

James Oh Email: james.oh@duogreen.com Phone: (201) 9315724

Related Public Records

Same Entity

Duogreen Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3013023150 DUOGREEN INC. Fort Lee, NJ, US

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 3013318814. Last updated year: 2026. Please use registration number 3013318814 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.