CHANGZHOU MAOKANG MEDICAL PRODUCTS CO., LTD

FDA Device Registration & Listing · Changzhou Jiangsu, CN · Registration 3010623099

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
3010623099
FEI Number
3010623099
Entity Name
CHANGZHOU MAOKANG MEDICAL PRODUCTS CO., LTD
City/State/Country
Changzhou Jiangsu, CN
Establishment Address
No. 88 of Longxi Avenue Zhulin Town, Jintan District, Changzhou Jiangsu 213241, CN
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Changzhou Maokang Medical Products Co., Ltd (Owner Number: 10082365)
Owner / Operator Contact Address
No. 88 of Longxi Avenue Zhulin Town, Jintan District, Changzhou, CN-JS 213241, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Skin Protectant Wipe MediChoice Adhesive Remover Pad Sterile Lubricate Jelly Lubricate Jelly

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KXF Applicator, Absorbent Tipped, Non-Sterile General Hospital Class 1 880.6025 2021-07-16
NEC Bandage, Liquid, Skin Protectant General Hospital Class 1 880.5090 2024-02-04
KXG Applicator, Absorbent Tipped, Sterile General Hospital Class 1 880.6025 2021-08-25
KOX Solvent, Adhesive Tape General, Plastic Surgery Class 1 878.4730 2024-02-04
KMJ Lubricant, Patient General Hospital Class 1 880.6375 2024-01-04

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Changzhou Maokang Medical Products 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
K820587 Abco Dealers, Inc. WET PACK LINE OF PRODUCTS 1982-03-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010623099. Last updated year: 2026. Please use registration number 3010623099 when referencing this establishment in official correspondence.
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