Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003835287

FEI Number

3003835287

Entity Name

Zhejiang Wellong Medical Technology Co., Ltd

City/State/Country

Huzhou City Zhejiang, CN

Establishment Address

Lvshan Industrial Area, Changxing County, Huzhou City Zhejiang 313105, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Zhejiang Wellong Medical Technology Co., Ltd (Owner Number: 9052133)

Owner / Operator Contact Address

Lvshan Industrial Area, Changxing County, Huzhou City, CN-ZJ 313105, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Anti-Fog Face Shield, Anti-Fog Mask IV Dressing Anti-Fog Visor, Anti-Fog Glasses Incise Drapes Island Dressing, Non-woven Dressing, Alginate Pad Paper Tape, PE Tape, Silk Tape, Retention Sheet, Elastic Tape, Plastic Tape Eye Patch

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LYU	Accessory, Surgical Apparel	General, Plastic Surgery	Class 1	878.4040	2016-11-25
KMK	Device, Intravascular Catheter Securement	General Hospital	Class 1	880.5210	2011-12-08
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2010-06-01
FYE	Dress, Surgical	General, Plastic Surgery	Class 1	878.4040	2016-11-25
NAC	Dressing, Wound, Hydrophilic	General, Plastic Surgery	Class 1	878.4018	2016-11-25
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2007-06-19
HMP	Pad, Eye	General, Plastic Surgery	Class 1	878.4440	2016-11-25

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Mack Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

Zhejiang Wellong Medical Technology Co., Ltd

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21
K915446	Sun Glitz Corp.	STRETCH WRAP	1992-05-06
K833120	Acme United Corp.	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29
K870091	Avery Intl.	IV SECUREMENT DEVICE USING PCCE THERMO. FILM	1987-02-04

Similar Registrations

Registration Number	Establishment Name	Location
9680454	EMPRESAS IAI S DE RL DE C.V.	H. MATAMOROS Tamaulipas, MX
3010227982	Tianjin Zhengtian Medical Instrument Co., Ltd.	Tianjin, CN
3016871880	PRIMEX DESIGN & FABRICATION	Richmond, IN, US
3005360866	QEL DOMINICANA S.A.	ESPERANZA Valverde, DO
3010601984	Jiangsu Haize Medical Scientific Development Co.,Ltd.	Wuxi Jiangsu, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003835287. Last updated year: 2026. Please use registration number 3003835287 when referencing this establishment in official correspondence.