Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031218453

FEI Number

3031218453

Entity Name

GUANGDONG MEICEN MEDICAL EQUIPMENT CO., LTD.

City/State/Country

foshan Guangdong, CN

Establishment Address

Building 5 Wanyang Innovation Park No. 82 Xiaotang Industrial Avenue Shishan Town Nanhai District, foshan Guangdong 528222, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Guangdong Meicen Medical Equipment Co., Ltd. (Owner Number: 10090516)

Owner / Operator Contact Address

Building 5 Wanyang Innovation Park No. 82 Xiaotang Industrial Avenue Shishan Town Nanhai District, foshan, CN-GD 528222, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Thermoplastic Bolus Thermoplastic Sheet Materials Thermoplastic Masks Thermoplastic Splint Material Vacuum Cushions Thermoplastic Orthoses and Orthotic Components Patient Positioning Devices and Components for Radiotherapy Vacuum Pump

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IXG	Phantom, Anthropomorphic, Radiographic	Radiology	Class 1	892.1950	2024-04-08
IWY	Holder, Head, Radiographic	Radiology	Class 1	892.1920	2024-04-08
EPP	Splint, Nasal	Ear, Nose, Throat	Class 1	874.5800	2024-04-08
KXH	Cradle, Patient, Radiologic	Radiology	Class 1	892.1830	2024-04-08
NOC	Splint, Extremity, Non-Inflatable, External, Non-Sterile	General, Plastic Surgery	Class 1	878.3910	2024-04-08
IWE	Monitor, Patient Position, Light-Beam	Radiology	Class 1	892.5780	2024-04-08
IOQ	Bed, Flotation Therapy, Powered	Physical Medicine	Class 2	890.5170	2024-04-08

Official Correspondent

Chunyan Situ

US Agent Details

Cancan Huang Business: OSMUNDA TECHNOLOGY CO., LTD. Email: Sunny.Huang@Osmundacn.com Phone: (858) 3571157

Related Public Records

Same Entity

Guangdong Meicen Medical 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
K890935	Dermanetics Corp.	SYSTEM 3000 FLUIDIZED AIR BED	1989-03-15

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031218453. Last updated year: 2026. Please use registration number 3031218453 when referencing this establishment in official correspondence.