Shenzhen Jian Feng Electronic Technology Co., Ltd

FDA Device Registration & Listing · Shenzhen Guangdong, CN · Registration 3009488655

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009488655
FEI Number
3009488655
Entity Name
Shenzhen Jian Feng Electronic Technology Co., Ltd
City/State/Country
Shenzhen Guangdong, CN
Establishment Address
#901,Block A, Fubilun Industrial Park,Chaoyang Rd, Yanchuan Community,Yanluo Subdistrict,Bao an District, Shenzhen Guangdong 518104, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Shenzhen Jian Feng Electronic Technology Co. Ltd (Owner Number: 10042303)
Owner / Operator Contact Address
#901,Block A, Fubilun Industrial Park,Chaoyang Rd, Yanchuan Community,Yanluo Subdistrict,Bao'an District, Shenzhen, CN-GD 518104, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

TENS AND POWERED MUSCLE STIMULATOR: FM-B2403A,FM-B2402,FM-B2405,Pro6ABS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NGX Stimulator, Muscle, Powered, For Muscle Conditioning Physical Medicine Class 2 890.5850 2022-03-10
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2022-03-10

Official Correspondent

Feng Wen

US Agent Details

Jessie Yao Business: Medright Tech Inc Email: info@medright-tech.com Phone: (718) 2169957

Related Public Records

Same Entity

Shenzhen Jian Feng Electronic 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
K221200 Xbody Hungary Kft. XBody Go USA, XBody Pro USA 2023-01-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009488655. Last updated year: 2026. Please use registration number 3009488655 when referencing this establishment in official correspondence.
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