YIWU EZ TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · Jinhua Zhejiang, CN · Registration 3035140505

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
3035140505
FEI Number
3035140505
Entity Name
YIWU EZ TECHNOLOGY CO., LTD.
City/State/Country
Jinhua Zhejiang, CN
Establishment Address
Room 1507 15th Floor Building B6 Headquarter Economy Park Choujiang District Yiwu, Jinhua Zhejiang 322099, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Yiwu EZ Technology Co., Ltd. (Owner Number: 10094231)
Owner / Operator Contact Address
Room 1507 15th Floor Building B6 Headquarter Economy Park Choujiang District Yiwu, Jinhua, CN-ZJ 322099, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tattoo Power Supplies Tattoo Tubes Tattoo Machines Tattoo Inks Tattoo Kits Tattoo Needles:RL, RS, M1, M1C, CM, F, SF Tattoo Cartridge Needles:RL, RS, M1, M1C, CM, F, SF Permanent Makeup Pigments Tattoo Aftercare Cream Tattoo Stencil Gel

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GDF Guide, Needle, Surgical General, Plastic Surgery Class 1 878.4800 2025-11-19
MQX Needle, Acupuncture, Single Use General Hospital Class 2 880.5580 2025-11-19
PPM General Purpose Reagent Pathology Class 1 864.4010 2025-11-19
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2025-11-19

Official Correspondent

WEI TONG

US Agent Details

Wilson Li Business: REPF America LLC Email: qagujdsvvt@outlook.com Phone: (719) 2013315

Related Public Records

Same Entity

Yiwu EZ 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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3035140505. Last updated year: 2026. Please use registration number 3035140505 when referencing this establishment in official correspondence.
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