Data / Medical devices / China / Xiamen Weiyou Intelligent Technology Co.,Ltd
Xiamen Weiyou Intelligent Technology Co.,Ltd: FDA-registered device maker in xiamen Fujian, China, 7 510(k) clearances
Xiamen Weiyou Intelligent Technology Co.,Ltd is registered with the FDA (registration 3011539161) in xiamen Fujian, China. It lists 9 device types. The FDA files 7 510(k) clearances under its listings, the newest dated June 10, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011539161
- Address
- Unit 3 No. 6 Xianghong Road,Torch Hi-Tech Zone Industrial Park,Xiang'an District, xiamen Fujian, China, 361101
- Owner or operator
- Xiamen Weiyou Intelligent Technology Co.,Ltd (10059059)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer, Specification developer
- First device listed
- April 4, 2019
- Registered through
- 2026
- Brand names listed
- AC Compression Machine:VU-IPC01,VU-IPC02,VU-NIPC01,VU-NIPC02,VU-IPC03,VU-IPC04,VU-IPC06, Air Mattress with Pump (Model: VU-602/6007), Air Mattress with Pump (Model: VU-AMP01), Air Mattress with Pump (Model: VU-AMP02), Air Pressure Therapy System, Air Pressure Therapy System (Model: IPC06), Air Pressure Therapy System (Model: VU-AMP01), Air Pressure Therapy System (Model: VU-AMP02) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bed, Ac-Powered Adjustable Hospital | FNL | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Bed, Manual | FNJ | 1 | Manufacturer | accessdata.fda.gov |
| Exerciser, Powered | BXB | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Massager, Powered Inflatable Tube | IRP | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Mattress, Air Flotation, Alternating Pressure | FNM | 2 | Manufacturer | accessdata.fda.gov |
| Pack, Hot Or Cold, Water Circulating | ILO | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Sleeve, Limb, Compressible | JOW | 2 | Contract 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 |
|---|---|---|---|---|---|---|
| June 10, 2026 | K253919 | Cryo And Thermo Therapy System | IRP | Substantially Equivalent | Xiamen Weiyou Intelligent Technology Co., Ltd. | accessdata.fda.gov |
| April 30, 2026 | K253064 | Air Pressure Therapy System (VU-IPC8M); Air Pressure Therapy System (VU-IPC6M); Air Pressure Therapy System (VU-IPC4X) | IRP | Substantially Equivalent | Xiamen Weiyou Intelligent Technology Co., Ltd. | accessdata.fda.gov |
| January 13, 2025 | K243791 | Air Pressure Therapy System | IRP | Substantially Equivalent | Xiamen Weiyou Intelligent Technology Co., Ltd. | accessdata.fda.gov |
| November 18, 2024 | K243320 | Air Pressure Therapy System (VU-IPC04B) | IRP | Substantially Equivalent | Xiamen Weiyou Intelligent Technology Co., Ltd. | accessdata.fda.gov |
| June 14, 2024 | K233238 | Air Pressure Therapy System (Model:VU-IPC4M) | IRP | Substantially Equivalent | Xiamen Weiyou Intelligent Technology Co., Ltd. | accessdata.fda.gov |
| June 22, 2021 | K201935 | Air Pressure Therapy System | IRP | Substantially Equivalent | Xiamen Weiyou Intelligent Technology Co., Ltd. | accessdata.fda.gov |
| May 11, 2021 | K210967 | Air Pressure Therapy System: VU-IPC06 | IRP | Substantially Equivalent | Xiamen Weiyou Intelligent Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Pack, Hot Or Cold, Water Circulating
- All makers of Bed, Manual
- All makers of Mattress, Air Flotation, Alternating Pressure
- All makers of Massager, Powered Inflatable Tube
- All makers of Bed, Ac-Powered Adjustable Hospital
- All makers of Lamp, Infrared, Therapeutic Heating
Updated June 10, 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.