Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3021599320

FEI Number

3021599320

Entity Name

LIFEMOTION MEDICAL TECHNOLOGY CO., LTD.

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

Bldg. 6, Baoxing Wisdom City, No. 650 Zhoushi Road, Bao'An District, Shenzhen, PEOPLE'S REPUBLIC OF CHINA, Shenzhen Guangdong 518126, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Lifemotion Medical Technology Co., Ltd. (Owner Number: 10083864)

Owner / Operator Contact Address

Bldg. 6, Baoxing Wisdom City, No. 650, Zhoushi Road, Bao'An District, Shenzhen, PEOPLE'S REPUBLIC OF CHINA, Shenzhen, CN-GD 518126, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K253838

PMA Number

N/A

All Registered Proprietary Names

Lifemotion Disposable Membrane Oxygenator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DTZ	Oxygenator, Cardiopulmonary Bypass	Cardiovascular	Class 2	870.4350	2026-05-09

Official Correspondent

Yang Liu

US Agent Details

Melissa DeHass Business: MEDIcept Inc Email: mdehass@medicept.com Phone: (717) 4760702

Related Public Records

Same Entity

Lifemotion Medical 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 3021599320. Last updated year: 2026. Please use registration number 3021599320 when referencing this establishment in official correspondence.