Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014315088

FEI Number

3014315088

Entity Name

JINGFANG PRECISION MEDICAL DEVICE(SHENZHEN) CO., LTD.

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

301 Bldg C & 401 Bldg A, Jinweiyuan, No.41 Qingsong Rd, Zhukeng Community, Longtian Street, Pingshan District, Shenzhen Guangdong 518118, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

JingFang Precision Medical Device(Shenzhen) Co., Ltd. (Owner Number: 10056834)

Owner / Operator Contact Address

301 Bldg C & 401 Bldg A, Jinweiyuan, No.41 Qingsong Rd, Zhukeng Community, Longtian Street, Pingshan District, 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

Reusable Needle Guides Disposable Needle Guides Biopsy Needle Guide Kit Disposable Needle Guides Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OIJ	Biopsy Needle Guide Kit	Radiology	Class 2	892.1560	2018-01-21

Official Correspondent

Junhua Zeng

US Agent Details

Weian Huang Business: JOYSUN USA LLC Email: weian@isosh.com Phone: (949) 4624543

Related Public Records

Same Entity

JingFang Precision Medical Device(Shenzhen) Co., Ltd.

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014315088. Last updated year: 2026. Please use registration number 3014315088 when referencing this establishment in official correspondence.