# Beijing Winkonlaser Technology Limited (manufacturer, Beijing, CN): 5 new FDA device listings, incl. stimulator, muscle, powered, for muscle conditioning

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Beijing Winkonlaser Technology Limited |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device; Export Device to the United States But Perform No Other Operation on Device |
| Location | Beijing, CN |
| New listings | 5 |
| Devices | Stimulator, Muscle, Powered, For Muscle Conditioning; Powered Laser Surgical Instrument; Powered Laser Surgical Instrument With MicrobeamFractional Output |
| Product codes | NGX, GEX, ONG |
| Device classes | Class II |
| Medical specialties | Physical Medicine, General, Plastic Surgery |
| Brand names | High Intensity Focused Electromagnetic Stimulation Device; Long Pulse Nd: YAG Laser System; Picosecond Laser System,LG002B,EL400,EL500,EL950,EL1200,EL1600,EL1800; Fractional CO2 Laser Therapy System,FC100, FC200, FC300,FC400,FC600,FC700 |
| First new listing | 2026-05-28 |
| Latest new listing | 2026-08-18 |
| FDA registration number | 3015452693 |
| 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: 2026-10-28T20:51:27.468Z.
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.