Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013947859

FEI Number

3013947859

Entity Name

GUANGDONG HUILIN PACKAGING TECHNOLOGY GROUP CO., LTD

City/State/Country

DongGuan Guangdong, CN

Establishment Address

Building 2, No. 20 Dakang Rd, Qiaotou Town, DongGuan Guangdong 523525, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

GUANGDONG HUILIN PACKAGING TECHNOLOGY GROUP CO., LTD (Owner Number: 10055647)

Owner / Operator Contact Address

Building 2, No. 20 Dakang Rd, Qiaotou Town, DongGuan, CN-GD 523525, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

BASIN, EMESIS-BODY WASTE RECEPTACLE TRAY, SURGICAL, INSTRUMENT

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FNY	Basin, Emesis	General Hospital	Class 1	880.6730	2019-07-30
LRP	Tray, Surgical	General, Plastic Surgery	Class 1	878.4800	2017-08-31

Official Correspondent

WEILING MO

US Agent Details

Roy Zhang Business: RGLM Consulting LLC Email: admin@rglm-fda.com Phone: (425) 2364274

Related Public Records

Same Entity

GUANGDONG HUILIN PACKAGING TECHNOLOGY GROUP 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
K881095	CooperVision, Inc.	KOI(TM) INSTRUMENT TRAYS	1988-04-06

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0036-2010	Alphatec Spine, Inc.	1	ROC Lumbar bolt caddy, Part Number: 81997-01-05. Sterilization container for ROC bolts/screws. Product is used to contain spinal implants.

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1062671	KENTRON HEALTH CARE, INC.	SPRINGFIELD, TN, US
3006487092	ELTEK INSTRUMENTS (PVT.) LTD.	Sialkot Punjab, PK
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013947859. Last updated year: 2026. Please use registration number 3013947859 when referencing this establishment in official correspondence.