Lifemotion Medical Technology Co., Ltd.
Manufacturer and brand owner in Shenzhen, Guangdong, China. 2 device types, 2 products catalogued, 1 clearance.
Lifemotion Medical Technology Co., Ltd. is a contract manufacturer holding a current FDA establishment registration. The registration covers Oxygenator, Cardiopulmonary Bypass, Accessory Equipment, Cardiopulmonary Bypass. 2 of its products are catalogued under its own name. Its earliest product listing with the FDA dates from 2021.
Registration
| Registered name | LIFEMOTION MEDICAL TECHNOLOGY CO., LTD. |
|---|---|
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3021599320 |
| FEI number | 3021599320 |
| DUNS | 698655611 |
| Establishment type | Contract manufacturer, Manufacturer, Exporter |
Chinese Registration
| Chinese legal name | 深圳汉诺医疗科技股份有限公司 |
|---|---|
| Unified social credit code | 91440300MA5F4BYR9M |
| Source | export sales certificate, Guangdong medical products administration |
Location
| City | Shenzhen |
|---|---|
| Province | Guangdong |
| Address | Bldg. 6, Baoxing Wisdom City, No. 650 Zhoushi Road, Bao’An District, Shenzhen, PEOPLE’S REPUBLIC OF CHINA |
| Postal code | 518126 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Accessory Equipment, Cardiopulmonary Bypass | Class 1 | Standalone Oxygenator Holder, LMF-13-001, Lifemotion Cart, LMF-10-001 | 2021 | 1 |
| Oxygenator, Cardiopulmonary Bypass | Class 2 | Lifemotion Disposable Membrane Oxygenator | 2026 | 1 |
Own-Brand Listings
| Product | Code | Catalogue numbers |
|---|---|---|
| Lifemotion | KRI | 2 |
| Lifemotion | DTZ | 1 |
Clearances
| Clearance | Decision date | Product code | Route | Held by |
|---|---|---|---|---|
| K253838 | 2026-03-16 | DTZ | Traditional | This company |
From the Company
Published by the company on its own website, not by the FDA.
| Founded | 2018 |
|---|---|
| Main products | ECMO system, Oxygenator, Centrifugal pump, Intelligent monitoring system, Cannula |
| Certifications | NMPA (China), CE MDR (EU), Patents in China, EU, Japan, USA |
| Export markets | Europe, Latin America, Africa, Asia |
Nearby Manufacturers
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.
The manufacturer named here can complete this record.