# Xiamen Weiyou Intelligent Technology Co.,Ltd (manufacturer, xiamen Fujian, CN): 4 new FDA device listings, incl. massager, powered inflatable tube

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Xiamen Weiyou Intelligent Technology Co.,Ltd |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device; Develop Specifications But Do Not Manufacture At This Facility |
| Location | xiamen Fujian, CN |
| New listings | 4 |
| Devices | Massager, Powered Inflatable Tube; Pack, Hot Or Cold, Water Circulating; Lamp, Infrared, Therapeutic Heating |
| Product codes | IRP, ILO, ILY |
| Device classes | Class II |
| Medical specialties | Physical Medicine |
| Brand names | Cryo And Thermo Therapy System (VU-COTO1-V1, VU-COT01-V2, VU-COT02, VU-COT03, Force-X CX5, Force-X CX7); Air Pressure Therapy System (VU-IPC8M, VU-IPC6M, VU-IPC4X); Red Light Hair Cap, Red Light Therapy Belt, Red Light Therapy Sleeping Bag, Red Light Therapy For Body,; Red Light Therapy Mat, Red Light Therapy Hands, Red Lgiht Therapy For Knee, Red Light Therapy Lamp, Heating Waist Belt); Heating Vibration Massage Shoulder, Heating Vibration Massage Wrist, Neck Heating Massage, Foot Heating Massage,; Heating Sleeping Bag, Heating Ankles, Heating Neck, Heating Knee Pad, Foot Heating, Heating Shoulder,; Red & Near-Infrared Light Therapy wraps/mats/pads (Heating Vibration Massage Elbow, Heating Vibration Massage knee Pad, |
| First new listing | 2026-05-25 |
| Latest new listing | 2026-07-15 |
| FDA registration number | 3011539161 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.