Hayco Enterprises (Shenzhen) Ltd.

FDA Device Registration & Listing · Shenzhen Guangdong, CN · Registration 3003889521

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
3003889521
FEI Number
3003889521
Entity Name
Hayco Enterprises (Shenzhen) Ltd.
City/State/Country
Shenzhen Guangdong, CN
Establishment Address
B7 and B6, Hayco Factory South No.7 Gate, Changdi Road, Yanchuan, Yanluo, Baoan District, Shenzhen Guangdong 518105, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
HAYCO MANUFACTURING LIMITED (Owner Number: 9052420)
Owner / Operator Contact Address
FLAT/RM 3002 30/F, CITICORP CENTRE, 18 WHITFIELD ROAD, CAUSEWAY BAY, HK, CN-NOTA 999077, 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
JES Floss, Dental Dental Class 1 872.6390 2019-09-16

Official Correspondent

Alex Zhang

US Agent Details

Victoria Pankovich Business: EAS Consulting Group, LLC. Email: usagent@easconsultinggroup.com Phone: (571) 4475500

Related Public Records

Same Entity

HAYCO MANUFACTURING LIMITED
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3015542695 Hayco Dominican Republic Co., S.R.L. Santo Domingo Este, DO
1000634183 Hayco Industries (Shenzhen) Ltd. Shenzhen Guangdong, CN

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
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 3003889521. Last updated year: 2026. Please use registration number 3003889521 when referencing this establishment in official correspondence.
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