Data / Medical devices / China / Lifemotion Medical Limited.
Lifemotion Medical Limited.: FDA-registered device maker in Hong Kong, China, 1 510(k) clearance
Lifemotion Medical Limited. is registered with the FDA (registration 3045892899) in Hong Kong, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 16, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3045892899
- Address
- Flat 6 11/F, Ming Fat Industrial Centre, 1kin Fat Street, Tuen Mun New Territories, Hong Kong, China, HK
- Owner or operator
- Lifemotion Medical Technology Co., Ltd. (10083864)
- Roles
- Exporter to the US
- First device listed
- December 24, 2021
- Registered through
- 2026
- Brand names listed
- Lifemotion Cart, LMF-10-001, Lifemotion Disposable Membrane Oxygenator, Standalone Oxygenator Holder, LMF-13-001
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory Equipment, Cardiopulmonary Bypass | KRI | 1 | Exporter to the US | accessdata.fda.gov |
| Oxygenator, Cardiopulmonary Bypass | DTZ | 2 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 16, 2026 | K253838 | Lifemotion Disposable Membrane Oxygenator | DTZ | Substantially Equivalent | Lifemotion Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Oxygenator, Cardiopulmonary Bypass
- All makers of Accessory Equipment, Cardiopulmonary Bypass
Updated March 16, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.