Data / Medical devices / China / Chengdu Cryo-Push Medical Technology Co.,ltd
Chengdu Cryo-Push Medical Technology Co.,ltd: FDA-registered device maker in CHENGDU Sichuan, China, 4 510(k) clearances
Chengdu Cryo-Push Medical Technology Co.,ltd is registered with the FDA (registration 3011491271) in CHENGDU Sichuan, China. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated April 3, 2026. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3011491271
- Address
- 2, Zone 9 and 102,105,Zone 20, Huayin Industrial Port, No.618, KeXing Road(West), Wenjiang District, CHENGDU Sichuan, China, 611137
- Owner or operator
- CHENGDU CRYO-PUSH MEDICAL TECHNOLOGY CO.,LTD (10051788)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- May 9, 2016
- Registered through
- 2026
- Brand names listed
- Anti-slip Waterproof Cast & Bandage Cover, Cold Compression Wrap 2, Cold Compression Wrap Pro, Cold Therapy System, Cold Therapy System Evo, Cold Therapy System II, Cold Therapy System III, CryoRx, Pulse Cold Compression Therapy System, MOD: KRP/MYY-M and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cover, Cast | KIA | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Massager, Powered Inflatable Tube | IRP | 2 | Manufacturer | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Pack, Hot Or Cold, Water Circulating | ILO | 2 | Contract manufacturer, Manufacturer | 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 |
|---|---|---|---|---|---|---|
| April 3, 2026 | K252386 | Hot and Cold Compression System (A02-C-032) | IRP | Substantially Equivalent | Chengdu Cryo-Push Medical Technology Co.,Ltd | accessdata.fda.gov |
| April 2, 2026 | K253076 | Cryopush Cold Compression Device (A02-P-001) | IRP | Substantially Equivalent | Chengdu Cryo-Push Medical Technology Co.,Ltd | accessdata.fda.gov |
| January 19, 2024 | K230524 | Cold Compression Wrap Pro | IRP | Substantially Equivalent | Chengdu Cryo-Push Medical Technology Co.,Ltd | accessdata.fda.gov |
| December 5, 2022 | K222669 | Cryopush Cold Compression Device | IRP | Substantially Equivalent | Chengdu Cryo-Push Medical Technology Co.,Ltd | accessdata.fda.gov |
Compare with other makers
- All makers of Pack, Hot Or Cold, Reusable
- All makers of Massager, Powered Inflatable Tube
- All makers of Pack, Hot Or Cold, Water Circulating
- All makers of Cover, Cast
Updated April 3, 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.