Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012324979

FEI Number

3012324979

Entity Name

SHENZHEN FENDA TECHNOLOGY CO., LTD.

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

Fenda Hi-Tech Park Zhoushi Road Shiyan, BaoAn, Shenzhen Guangdong 518108, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

SHENZHEN FENDA TECHNOLOGY CO., LTD. (Owner Number: 10051582)

Owner / Operator Contact Address

Fenda Hi-Tech Park, Zhoushi Road Shiyan, Bao'an, Shenzhen, CN-GD 518108, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ActiGraph LEAP

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LEL	Device, Sleep Assessment	Neurology	Class 2	882.5050	2024-05-09

Official Correspondent

ADEE LIU

US Agent Details

Jessie Peng Business: Mars Business Consulting, LLC Email: jessie@registeragentllc.com Phone: (858) 9050218

Related Public Records

Same Entity

SHENZHEN FENDA TECHNOLOGY 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 3012324979. Last updated year: 2026. Please use registration number 3012324979 when referencing this establishment in official correspondence.