Data / Medical devices / China / Resvent Medical Technology Co., Ltd.
Resvent Medical Technology Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Resvent Medical Technology Co., Ltd. is registered with the FDA (registration 3019793765) in Shenzhen Guangdong, China. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 23, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3019793765
- Address
- BC601, Gaoxinqi Factory, District 67 Xingdong Community,Xinan Street, Baoan District, Shenzhen Guangdong, China, 518100
- Owner or operator
- Resvent Medical Technology Co., Ltd. (10082384)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- July 19, 2021
- Registered through
- 2026
- Brand names listed
- Disposable Anesthesia Breathing Circuit, IBreeze 30STA Device (IBreeze 30STA), RXiBreeze 20C, RXiBreeze PAP System, ResAssist, Tube, iBreeze PAP (iBreeze 20A; iBreeze 25ST; iBreeze 25STA), iMatrix Sleeping Management Software
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Circuit, Breathing (W Connector, Adaptor, Y Piece) | CAI | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Continuous Ventilator, Minimal Ventilatory Support | QOR | N | Manufacturer | accessdata.fda.gov |
| Medical Device Data System | OUG | 1 | Manufacturer | accessdata.fda.gov |
| Non-Continuous Ventilator For Emergency Use | QOQ | N | Manufacturer | accessdata.fda.gov |
| Support, Breathing Tube | JAY | 1 | Manufacturer | accessdata.fda.gov |
| Ventilator, Non-Continuous (Respirator) | BZD | 2 | 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 |
|---|---|---|---|---|---|---|
| July 23, 2026 | K253044 | RXiBreeze PAP System (RXiBreeze 20C) | BZD | Substantially Equivalent | Resvent Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Support, Breathing Tube
- All makers of Medical Device Data System
- All makers of Continuous Ventilator, Minimal Ventilatory Support
- All makers of Circuit, Breathing (W Connector, Adaptor, Y Piece)
- All makers of Ventilator, Non-Continuous (Respirator)
Updated July 23, 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.