Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009515470

FEI Number

3009515470

Entity Name

ADVANCE TECHNOLOGY LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

B301,B205-210, building 13, Zhonghaixin innovation industry city, no.12,, Ganli sixth road, Gankeng community, Jihua street, Longgang district, Shenzhen, Shenzhen Guangdong 518112, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

ADVANCE TECHNOLOGY LTD (Owner Number: 10039324)

Owner / Operator Contact Address

6/F,UNIT13-15,GRAND CITY PLAZA NO.1, SAI LAU KOK ROAD,TSUEN WAN,, TSUEN WAN,, CN-HK 999077, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Marlincare Oral B AquaCare Advanced V-Go Disposable Insulin Delivery Device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JEQ	Toothbrush, Powered	Dental	Class 1	872.6865	2024-11-05
EFS	Unit, Oral Irrigation	Dental	Class 1	872.6510	2020-06-02
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2012-06-12
LZG	Pump, Infusion, Insulin	General Hospital	Class 2	880.5725	2012-06-12

Official Correspondent

Honghai Du

US Agent Details

Brett Freeman Email: bfreeman@providence-connect.com Phone: (949) 8518888

Related Public Records

Same Entity

ADVANCE TECHNOLOGY 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
K844318	Pro Pulse, Inc.	ORAL IRRIGATION TIP	1984-11-23
K221518	Np Medical	NP Medical nCompass Extension Set with Stabilizing Base	2022-11-03
K953474	Medikmark, Inc.	IV START KIT	1995-10-02
K972493	Nipro Medical Corp.	NIPRO DISPOSABLE SOLUTION INFUSION SET	1997-09-18
K982672	Baxter Healthcare Corp	COLLEAGUE PUMP SYRINGE ADAPTER SET	1998-09-04

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0010-2025	Smiths Medical ASD Inc.	2	CADD Medication Cassette Reservoir, 100mL, Product Code 21-7002-24
Z-0011-2025	Smiths Medical ASD Inc.	2	CADD Medication Cassette Reservoir, 100mL, FS, Product Code 21-7302-24
Z-0012-2013	Baxter Healthcare Corp. Rt.	2	Baxter Interlink System Buretrol Solution Set with 150 mL Burette (Ball-Valve Drip Chamber); a sterile Rx IV fluid pathway device. Product Usage: The device is used for the administration of fluids from a container into the patient's vascular system through a vascular access device.
Z-0012-2025	Smiths Medical ASD Inc.	2	CADD Medication Cassette Reservoir, 100mL, FS, YELLOW, Product Code 21-7300-24
Z-0013-2013	Baxter Healthcare Corp. Rt.	2	Baxter Interlink System Buretrol Solution Set, 117" (3.0 m), with 150 mL Burette (Ball-Valve Drip Chamber) (Non-DEHP); a sterile Rx IV fluid pathway device; Product Usage: The device is used for the administration of fluids from a container into the patient's vascular system through a vascular access device.

Similar Registrations

Registration Number	Establishment Name	Location
3015925939	EXPEDITORS	Surprise, AZ, US
3020145267	Shanghai Shi Mian De Electronic Products Co. Ltd.	Jinshan District Shanghai, CN
3029987245	FLAUS, INC.	New York, NY, US
3013257234	MINGZHEN (DONGGUAN) ELECTRONICS CO., LTD	Dongguan Guangdong, CN
3038200340	WEIFANG YANGXU LABOR PROTECTION PRODUCTS CO., LTD	Weifang Shandong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009515470. Last updated year: 2026. Please use registration number 3009515470 when referencing this establishment in official correspondence.