# Beijing Sanhe Laser Co., Ltd. (foreign exporter, Beijing, CN): 6 new FDA device listings, incl. powered laser surgical instrument

**Score:** 55/100

| Field | Value |
|---|---|
| Establishment | Beijing Sanhe Laser Co., Ltd. |
| Role | Foreign exporter |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device |
| Location | Beijing, CN |
| New listings | 6 |
| Devices | Powered Laser Surgical Instrument; Stimulator, Muscle, Powered, For Muscle Conditioning |
| Product codes | GEX, NGX |
| Device classes | Class II |
| Medical specialties | General, Plastic Surgery, Physical Medicine |
| Brand names | Cryojet Plus (SHE-ACP001-1); CO2 Laser Therapy Systems (SHE-LSP003-1); HI-EMT MAGSHAPE(SHE-MSP003/SHE-MSP001/SHE-MSP002); Diode Laser Hair Removal System(P-808/P-808L/P-808S/P-808W); LumiGlam Laser System (SHE-LSP601-3); Q-Switched Nd:YAG Laser (SHE-LSP101-1) |
| First new listing | 2026-06-11 |
| Latest new listing | 2026-06-11 |
| FDA registration number | 3048246437 |
| Registration expires | 2026-12-31 |

## Why this score
- 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.