Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015335977

FEI Number

3015335977

Entity Name

HE CHUANG PLASTIC & RUBBER CO., LTD

City/State/Country

Zibo Shandong, CN

Establishment Address

Lot 2, No. 21 Qingtian Road, Qilu Chemical Industrial Park, Zibo Shandong 255414, CN

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

He Chuang Plastic & Rubber Co., Ltd (Owner Number: 10060105)

Owner / Operator Contact Address

Lot 2, No. 21 Qingtian Road, Qilu Chemical Industrial Park, Zibo, CN-SD 255414, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K220228

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
OPJ	Medical Gloves With Chemotherapy Labeling Claims - Test For Use With Chemotherapy Drugs	General Hospital	Class 1	880.6250	2022-12-28
QDO	Fentanyl And Other Opioid Protection Glove	General Hospital	Class 1	880.6250	2022-12-28
LZC	Medical Glove, Specialty	General Hospital	Class 1	880.6250	2022-12-28
LZA	Polymer Patient Examination Glove	General Hospital	Class 1	880.6250	2022-12-28
OPJ	Medical Gloves With Chemotherapy Labeling Claims - Test For Use With Chemotherapy Drugs	General Hospital	Class 1	880.6250	2024-08-27
LZA	Polymer Patient Examination Glove	General Hospital	Class 1	880.6250	2024-08-27
LZC	Medical Glove, Specialty	General Hospital	Class 1	880.6250	2024-08-27

Official Correspondent

Coco Wang

US Agent Details

Ken Li Business: Omni International Corp Email: like@bluesail.cn Phone: (603) 4711499

Related Public Records

Same Entity

He Chuang Plastic & Rubber 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
K212801	Hong Seng Gloves Sdn Bhd	Powder free nitrile examination glove- black, non sterile	2022-01-09
K260806	Vista Industries,, LLC	Nitrile Disposable Examination Gloves	2026-06-03
K011593	Ansell Healthcare Products, Inc.	MICRO-TOUCH NITRILE POWDER FREE SYNTHETIC MEDICAL EXAMINATION GLOVES, COLOR BLUE NON-STERILE	2001-06-21
K981039	Sri Johani Sdn. Bhd.	POWDERFREE GREEN NITRILE EXAMINATION GLOVES (POLYMER COATED)	1998-04-21
K101595	Better Care Plastic Technology Cp., Ltd.	POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE	2010-08-06

Similar Registrations

Registration Number	Establishment Name	Location
3030671502	GUANGDONG VYIMED CO., LTD.	Qingyuan Guangdong, CN
3026062711	RMKH GLOVE (CAMBODIA) CO., LTD.	Bavet City Svay Rieng, KH
3043739177	US Paper Mill LLC	Chillicothe, OH, US
3013681444	ANREL DISTRIBUTION LLC	Jackson, NJ, US
3022543478	SHANDONG BLUE SAIL HEALTH TECHNOLOGY CO., LTD	Weifang Shandong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015335977. Last updated year: 2026. Please use registration number 3015335977 when referencing this establishment in official correspondence.