SHENZHEN WOODPECKER TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · Shenzhen City Guangdong, CN · Registration 3043749713

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
3043749713
FEI Number
3043749713
Entity Name
SHENZHEN WOODPECKER TECHNOLOGY CO., LTD.
City/State/Country
Shenzhen City Guangdong, CN
Establishment Address
1301, Xinghe Times Building, Dalang North Road, Dalang Community, Dalang Street, Longhua District, Shenzhen City Guangdong 518000, CN
Establishment Type(s)
Remanufacture Medical Device,Repack or Relabel Medical Device,Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Foreign Private Label Distributor,Manufacture Medical Device,Reprocess Single-Use Device
Owner / Operator
Shenzhen Woodpecker Technology Co., Ltd. (Owner Number: 10095234)
Owner / Operator Contact Address
1301, Xinghe Times Building, Dalang North Road, Dalang Community, Dalang Street, Longhua District, Shenzhen City, CN-GD 518000, CN
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
EFS Unit, Oral Irrigation Dental Class 1 872.6510 2026-02-10
JES Floss, Dental Dental Class 1 872.6390 2026-02-10

Official Correspondent

Guorong Wang

US Agent Details

Jessica Zhong Business: UA INTERNATIONAL INC. Email: UA.customerservice@hotmail.com Phone: (719) 6787182

Related Public Records

Same Entity

Shenzhen Woodpecker 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
K844318 Pro Pulse, Inc. ORAL IRRIGATION TIP 1984-11-23
K882164 Arthur Blank & Co., Inc. FLOSS CARD 1988-06-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043749713. Last updated year: 2026. Please use registration number 3043749713 when referencing this establishment in official correspondence.
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