# Guangzhou Niansheng Beauty Equipment Co., Ltd. (contract manufacturer, Guangzhou Guangdong, CN): 4 new FDA device listings, incl. guide, needle, surgical

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Guangzhou Niansheng Beauty Equipment Co., Ltd. |
| Owner / operator | Beijing Niansheng Beauty Technology Co., Ltd. |
| Role | Contract manufacturer |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Guangzhou Guangdong, CN |
| New listings | 4 |
| Devices | Guide, Needle, Surgical; Stimulator, Muscle, Powered, For Muscle Conditioning; Powered Laser Surgical Instrument; Marker, Skin |
| Product codes | GDF, NGX, GEX, FZZ |
| Device classes | Class I, Class II |
| Medical specialties | General, Plastic Surgery, Physical Medicine |
| Brand names | NS Multifunctional device ,NS-D5,LS-E120,LS-B505,NS-M2,LS-M107,LS-NS210,NS-M9,NS-B17,LS-D12,; LS-NS222,LS-NS221,LS-NS219,NS-M23,NS-M20,NS-M19,NS-M17,NS-M4,NS-Q4,NS-Q5,NS-Q6,NS-Q7,NS-Q8; LS-Y8, NS-D3, LS-NS227, LS-NS220, NS-D2, NS-D11,NS-D12, LS-Y8C, LS-Y8A, NS-D43, NS-D49,NS-D50,NS-D51,NS-D52,NS-D53; Multifunctional Laser Beauty Machine:NS Pico Laser,ND YAG,NS-D4,NS-D10,LS-NS22,LS-NS23,LS-NS230,NS-Y26,NS-D15,LS-NS24,; LS-C6,LS-C7,LS-NS227,LS-NS229,LS-NS214,NS-D01,NS-Q3A,NS-Q3,NS-D16,NS-D5,NS-Q2,NS-Q1,; NS shockware,LS-F219,LS-F221,LS-F222,LS-F213,NS-J3,LS-F214,NS-J4,LS-F218,LS-L003,NS-L1,LS-L009,; NS-B70,NS-J12,NS-N21,NS-N20,NS-N12,NS-N2B,NS-J25,NS-J26,NS-J27,NS-J28,NS-J29; EMS4A,EMS4A-1,EMS4A-2,LS-B174B,LS-B174A,NS-B174C,NS-B31A,NS-B31B,NS-B31C,NS-B37,NS-B21,NS-B21A,NS-B22,NS-P5, |
| First new listing | 2026-05-16 |
| Latest new listing | 2026-05-16 |
| FDA registration number | 3013503862 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- 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.