Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011247798

FEI Number

3011247798

Entity Name

JIANGSU YIZHENG CAREPRO MEDICAL INSTRUMENTS CO., LTD.

City/State/Country

Yizheng Jiangsu, CN

Establishment Address

No.3 Jingxiu Road, Yizheng Economic Development Zone, Yizheng Jiangsu 211400, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Jiangsu Yizheng Carepro Medical Instruments Co., Ltd. (Owner Number: 10047612)

Owner / Operator Contact Address

No.3 Jingxiu Road, Yizheng Economic Development Zone, Yizheng, CN-JS 211400, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Hydrocolloid Dressings Adhesive Tapes and Bandage, Pressure strip, Pressure wrap, Breath Tape (Mouth Tape, Sleep Tape, Nose Tape, Nasal Strips) eye shield Wound Dressing, Foam Dressings, Silicone Foam Dressings First Aid Kit with drug

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NAE	Dressing, Wound, Hydrogel Without Drug And/Or Biologic	General, Plastic Surgery	Class 1	878.4022	2024-04-26
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2014-10-12
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2016-12-12
NAC	Dressing, Wound, Hydrophilic	General, Plastic Surgery	Class 1	878.4018	2023-07-04
LRR	First Aid Kit With Drug	Unknown	Class N	N/A	2025-11-30

Official Correspondent

Yongmei Yan

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

Jiangsu Yizheng Carepro Medical Instruments 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
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21
K915446	Sun Glitz Corp.	STRETCH WRAP	1992-05-06
K833120	Acme United Corp.	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29
K870091	Avery Intl.	IV SECUREMENT DEVICE USING PCCE THERMO. FILM	1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011247798. Last updated year: 2026. Please use registration number 3011247798 when referencing this establishment in official correspondence.