Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014233600

FEI Number

3014233600

Entity Name

SHENZHEN CORERAY TECHNOLOGY CO., LTD.

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

803-804 Chuangzhi Industrial Building, No.1 Yingai Road, Langkou Community, Dalang Street, Longhua District, Shenzhen Guangdong 518109, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shenzhen Coreray Technology Co., Ltd. (Owner Number: 10056465)

Owner / Operator Contact Address

803-804 Chuangzhi Industrial Building, No.1 Yingai Ro, Langkou Community, Dalang Street, Longhua District, Shenzhen, CN-GD 518109, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K172797

PMA Number

N/A

All Registered Proprietary Names

ECG Electrode Flexible Video Laryngoscope CR-33/ CR-33D/ CR-33H/ CR-33HD/ CR-33CHD Flexible Video Laryngoscope CR-33R/ CR-33RD/ CR-33HR/ CR-33P/ CR-33U/ CR-33UD/ CR-33HU/ CR-33C/ CR-33CD/ CR-33HC Video Otorhinolaryngoscope CR-31O Nasal Oxygen Cannula Patient Monitoring Cable (SpO2 Extension Cable) ECG Cable/Leadwires

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DRX	Electrode, Electrocardiograph	Cardiovascular	Class 2	870.2360	2017-12-12
CAL	Laryngoscope, Non-Rigid	Anesthesiology	Class 1	868.5530	2018-12-04
ERA	Otoscope	Ear, Nose, Throat	Class 1	874.4770	2020-11-24
CAT	Cannula, Nasal, Oxygen	Anesthesiology	Class 1	868.5340	2019-10-25
DSA	Cable, Transducer And Electrode, Patient, (Including Connector)	Cardiovascular	Class 2	870.2900	2020-06-29
DSA	Cable, Transducer And Electrode, Patient, (Including Connector)	Cardiovascular	Class 2	870.2900	2018-03-06

Official Correspondent

SIMON FAN

US Agent Details

Andy Smith Business: GRZAN GROUP INC. Email: info@grzan-ar.com Phone: (332) 2015192

Related Public Records

Same Entity

Shenzhen Coreray 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
K934333	3M Medical Products Group	3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE	1994-07-07
K932506	Rudolf Riester GmbH & Co. KG	RI-SCOPE (S)	1993-10-08
K880323	Medtronic Vascular	MEDTRONIC MODEL 5411 SURGICAL CABLE ADAPTOR	1988-03-22

Similar Registrations

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3013873578	SHANGHAI YUECHEN MEDICAL SUPPLY CO..LTD.	Shanghai, CN
3003584029	Braemar Manufacturing, LLC	San Diego, CA, US
3017425211	LOHMANN PRECISION DIE CUTTING, LLC	Orange, VA, US
3008773647	CARDIONET, LLC	Phoenix, AZ, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014233600. Last updated year: 2026. Please use registration number 3014233600 when referencing this establishment in official correspondence.