Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013023150

FEI Number

3013023150

Entity Name

DUOGREEN INC.

City/State/Country

Fort Lee, NJ, US

Establishment Address

2460 lemoine Ave 302, Fort Lee, NJ 07024, US

Establishment Type(s)

Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

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

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
MSH	Respirator, Surgical	General, Plastic Surgery	Class 2	878.4040	2020-04-02
NAC	Dressing, Wound, Hydrophilic	General, Plastic Surgery	Class 1	878.4018	2019-07-09

Official Correspondent

JAMES OH

US Agent Details

No US Agent registered (Local establishment).

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
3013318814	DuoGreen Co., Ltd	Gangseo-gu Seoul, KR

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K102092	Prestige Ameritech	PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES	2010-10-06

Similar Registrations

Registration Number	Establishment Name	Location
3020623413	NITTA S.A.	Bogota, CO
3016765490	XIAMEN CHUANFUTANG PHARMACEUTICAL CO.,LTD	xiamen Fujian, CN
3041850200	RISKWISE SUPPLIES LLC	Lorton, VA, US
3018382937	MID-AMERICA SAFETY CORP	Elk Grove Village, IL, US
3010141571	Xiantao Zhongyi Safety & Protection Products Co.,Ltd.	Xiantao City Hubei, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013023150. Last updated year: 2026. Please use registration number 3013023150 when referencing this establishment in official correspondence.