JIUJIANG JIEBAO MEDICINE EQUIPMENT CO., LTD

FDA Device Registration & Listing · Jiujiang City Jiangxi, CN · Registration 3017166480

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
3017166480
FEI Number
3017166480
Entity Name
JIUJIANG JIEBAO MEDICINE EQUIPMENT CO., LTD
City/State/Country
Jiujiang City Jiangxi, CN
Establishment Address
No. 1, Xingyuan Road Branch 3, Lushan Industrial Park, Jiujiang City Jiangxi 332800, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Jiujiang Jiebao Medicine Equipment Co., Ltd (Owner Number: 10094839)
Owner / Operator Contact Address
No. 1, Xingyuan Road Branch 3, Lushan Industrial Park, Jiujiang City, CN-JX 332800, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pain Relief Patch, Acupoint Pressure Stimulation Patch Nasal Strips, Warm wood Patch, Mouth Tape, Kinesiology Tape, Facial Mask, Motion Sickness Patch, Foot Patch, Hand Patch, Vitamin patches, Essential Oil Patch, Mosquito Repellent Patch, Aromatic Patch Adhesive Bandage

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OMW Adhesive Backed Thermal Skin Patches Physical Medicine Class 1 890.5710 2025-12-29
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2025-12-29
FPX Strip, Adhesive, Closure, Skin General Hospital Class 1 880.5240 2025-12-29

Official Correspondent

Weifa Miao

US Agent Details

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

Related Public Records

Same Entity

Jiujiang Jiebao Medicine Equipment 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 3017166480. Last updated year: 2026. Please use registration number 3017166480 when referencing this establishment in official correspondence.
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