Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030656972

FEI Number

3030656972

Entity Name

SHENZHEN JUNYUAN MEDICAL EQUIPMENT CO., LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

Room 501, Building 1, No. 6352, Pingshan Avenue, Shatian Community, Kengzi Street, Pingshan District, Shenzhen, Shenzhen Guangdong 518118, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shenzhen JunYuan Medical Equipment Co., LTD (Owner Number: 10090285)

Owner / Operator Contact Address

Room 501, Building 1, No. 6352, Pingshan Avenue, Shatian Community, Kengzi Street, Pingshan District, Shenzhen, Shenzhen, CN-GD 518118, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Video Laryngoscopes M3R;Video Laryngoscopes M3D Flexible Videoscopes M3S Disposable anesthetic speculum MAC1;MAC2;MAC3;MAC4;MAC5 Endoscope Image Processor M10;Endoscope Image Processor M12;Endoscope Image Processor MCCU

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CAL	Laryngoscope, Non-Rigid	Anesthesiology	Class 1	868.5530	2024-03-07

Official Correspondent

No official correspondent registered.

US Agent Details

James Wang Email: fda-rep@llins-tech.com Phone: (720) 2171916

Related Public Records

Same Entity

Shenzhen JunYuan Medical Equipment Co., LTD

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3010202439	Karl Storz Endoscopy-America, Inc.	El Segundo, CA, US
3009420598	Primo Medical Group, Inc	W Bridgewater, MA, US
3003882387	B. ALI IMPEX	SIALKOT, Punjab, PK
3014233600	SHENZHEN CORERAY TECHNOLOGY CO., LTD.	Shenzhen Guangdong, CN
3009255580	SWENGG CO	Sialkot Punjab, PK

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030656972. Last updated year: 2026. Please use registration number 3030656972 when referencing this establishment in official correspondence.