HUA YI MANUFACTORY

FDA Device Registration & Listing · GUANGZHOU Guangdong, CN · Registration 3004593486

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
3004593486
FEI Number
3004593486
Entity Name
HUA YI MANUFACTORY
City/State/Country
GUANGZHOU Guangdong, CN
Establishment Address
DING ON LANE, No. 49 TAK SHING, CHUNG ROAD, RM 101, GUANGZHOU Guangdong --, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
HUA YI MANUFACTORY (Owner Number: 9064017)
Owner / Operator Contact Address
DING ON LANE, # 49 TAK SHING, CHUNG ROAD, RM 101, GUANGZHOU, CN-NOTA --, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tech-Med McKesson McKesson Tech-Med McKesson, Tech-Med

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KES Coverslips, Microscope Slide Pathology Class 1 864.3010 2008-09-03
FTY Tape, Measuring, Rulers And Calipers General, Plastic Surgery Class 1 878.4800 2005-08-01
HOX Chart, Visual Acuity Ophthalmic Class 1 886.1150 2004-06-08
OHY Pill Crusher/Cutter General Hospital Class 1 880.6430 2011-03-02

Official Correspondent

ALEX LUNG

US Agent Details

Wen Wang Email: Wen.Wang@WillowGlenFDA.com Phone: (619) 8690249

Related Public Records

Same Entity

HUA YI MANUFACTORY
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004593486. Last updated year: 2026. Please use registration number 3004593486 when referencing this establishment in official correspondence.
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