Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010142064

FEI Number

3010142064

Entity Name

POWERFIRST TECHNOLOGY COMPANY LIMITED

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

2nd Floor Lantian Bldg, KaiTian Science Park, Pinghu Street, Shenzhen Guangdong 518110, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

PowerFirst Technology Company Limited (Owner Number: 10042044)

Owner / Operator Contact Address

2nd Floor Lantian Bldg, KaiTian Science Park, Pinghu Street, Shenzhen, CN-GD 518110, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KNO	Accessories, Wheelchair	Physical Medicine	Class 1	890.3910	2012-10-10

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: David.Lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

PowerFirst Technology Company Limited

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 3010142064. Last updated year: 2026. Please use registration number 3010142064 when referencing this establishment in official correspondence.