Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042277643

FEI Number

3042277643

Entity Name

XIAMEN COSON MEDICAL INSTRUMENTS CO., LTD

City/State/Country

Xiamen City Fujian, CN

Establishment Address

2nd Floor, No. 89, Xiyuan Road, Xinyang Industrial Zone, Haicang District, Xiamen City Fujian 361028, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Xiamen COSON Medical Instruments Co., Ltd (Owner Number: 10094378)

Owner / Operator Contact Address

2nd Floor, No. 89, Xiyuan Road, Xinyang Industrial Zone, Haicang District, Xiamen City, CN-FJ 361028, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Sterile Exsanguination Tourniquet Disposable Sterile Anti-blocking Suction Tube Sterile Surgical Tissue Retractor Disposable Sterile Dilator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GAX	Tourniquet, Nonpneumatic	General, Plastic Surgery	Class 1	878.5900	2025-11-26
BYY	Tube, Aspirating, Flexible, Connecting	General Hospital	Class 2	880.6740	2025-11-26
GAD	Retractor	General, Plastic Surgery	Class 1	878.4800	2025-11-26

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Mack Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

Xiamen COSON 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
K922626	Andronic Devices, Ltd.	ADEPT INSTRUMENT POSITIONING ACCESSORY	1992-10-19
K820290	The Anspach Effort, Inc.	SELF RETAINING RETRACTOR FOR HAND SURG	1982-03-05
K760422	Cutter Laboratories, Inc.	SURGICAL RETRACTOR	1976-08-23

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0031-2014	Aesculap, Inc.	1	UNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments during surgical procedures.

Similar Registrations

Registration Number	Establishment Name	Location
3027555965	INNOVATE MEDICAL MALAYSIA, SDN. BHD.	Shah Alam Selangor, MY
3008973900	SAFECARE MEDICAL PRODUCTS CO., LTD. (HEFEI)	HEFEI Anhui, CN
3030461038	PLASTICOSCRT, S.A. DE C.V.	Santa Catarina Nuevo Leon, MX
3014146184	WHEELSTONE ENTERPRISE CO., LTD.	Taichung City, TW
3030191206	XMETIX LTD	Nazareth Northern, IL

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042277643. Last updated year: 2026. Please use registration number 3042277643 when referencing this establishment in official correspondence.