FDA device listing
Pico laser machine:A020,A043,A011,A32-7,C137,A509,G054,H001,PL01,PL02,PL03,PL04,PL05
FDA device listing 2041182828 · guangdong fuqiang beauty equipment co.,Limited
Key facts
| Proprietary names | Pico laser machine:A020,A043,A011,A32-7,C137,A509,G054,H001,PL01,PL02,PL03,PL04,PL05 |
|---|---|
| Owner/operator | guangdong fuqiang beauty equipment co.,Limited |
| Owner/operator number | 10094763 |
| Product codes | NXF |
| Device names | NXF - Gas, Laser Generating |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4810 |
| Review panels | General & Plastic Surgery |
| Registered establishments | GUANGDONG FUQIANG BEAUTY EQUIPMENT CO.,LIMITED |
| Establishment registrations | 3043140693 |
| FEI numbers | 3043140693 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database