Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008830133

FEI Number

3008830133

Entity Name

SHENZHEN AEON TECHNOLOGY CO.,LTD

City/State/Country

shenzhen Guangdong, CN

Establishment Address

A301, Building A, No. 5003, Bao'an Avenue, Bao'an District, shenzhen Guangdong 518126, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SHENZHEN AEON TECHNOLOGY CO.,LTD (Owner Number: 10052918)

Owner / Operator Contact Address

A301, Building A, No. 5003, Bao'an Avenue, Bao'an District, Shenzhen, CN-GD 518126, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Pulse Oximeter A310E, A320E, A330E, A340E, A310, A350, A350E, A370E, A371E, AIMO1, AIMO2 Compressor Nebulizer A500LWD01,A500LWD02,A500LWD04,A500LWD05,A500LWDC01,A500LWDC02,A500LWDC04,A500LWDC05 Fingtip Pulse Oximeter A310 Fingertip Pulse Oximeter A310B, A330B, A340B Infrared Thermometer A200,A201,A202,A201F,A201W,A202W,A202C,A202D,A202E,A202F Fingertip pulse oximeter A300,A310,A320,A330,A340,A350,A310L,A330N,A340L,A310E Electronic Thermometer A260, A261, A262, A263, A264, A265

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OCH	Oximeter, Infrared, Sporting, Aviation	Cardiovascular	Class 2	870.2700	2018-09-26
BTI	Compressor, Air, Portable	Anesthesiology	Class 2	868.6250	2016-10-18
DQA	Oximeter	Cardiovascular	Class 2	870.2700	2017-04-17
DQA	Oximeter	Cardiovascular	Class 2	870.2700	2020-09-23
FLL	Continuous Measurement Thermometer	General Hospital	Class 2	880.2910	2017-12-10
DQA	Oximeter	Cardiovascular	Class 2	870.2700	2019-09-16
SDV	Clinical Electronic Thermometer	General Hospital	Class 2	880.2910	2025-07-02

Official Correspondent

XIE HUA

US Agent Details

Raymond Xie Email: iamemocom@hotmail.com Phone: (510) 9347603

Related Public Records

Same Entity

SHENZHEN AEON TECHNOLOGY 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
K900686	Medical Industries America, Inc.	MAXI COMPRESSORS	1990-04-26
K903523	Hewlett-Packard Co.	HP MODEL M1020A, ARTERIAL OXYGEN SAT/PLETH MODULE	1990-10-23
K973147	Nellcor Puritan Bennett, Inc.	NPB-295 PULSE OXIMETER	1997-11-14
K231243	Guangdong Genial Technology Co., Ltd.	Finger Clip Pulse Oximeter	2023-10-31
K971628	Somanetics Corp.	SOMANETICS INVOS 3100A CEREBRAL OXIMETER (INVOS)	1997-10-10

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0020-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	CAPNOSTREAM 20 (US) N, Part Number CS08651
Z-0022-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-02
Z-0023-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-03
Z-0028-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	Capnostream20 (US) M, Part Number CS08653
Z-0029-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	Capnostream20 (US) M W/PRINTER, Part Number CS08659

Similar Registrations

Registration Number	Establishment Name	Location
3016170326	ZHUHAI LINTE MEDICAL INSTRUMENT CO., LTD.	Zhuhai Guangdong, CN
3013545943	Prime Med Shop LLC	Stafford, TX, US
3016859940	JIANGSU KONSUNG BIO-MEDICAL SCIENCE AND TECHNOLOGY CO LTD	Danyang Jiangsu, CN
3009327812	Proactive Medical Products	Mount Vernon, NY, US
3017207990	SHENZHEN YUEZHONGXING TECHNOLOGY CO.,LTD	Huizhou Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008830133. Last updated year: 2026. Please use registration number 3008830133 when referencing this establishment in official correspondence.