FDA device listing
Diode Laser Hair Removal System,Z820,Z860,Z840,Z870,Z890,,Long Pluse ND-YAG Alexandrite Laser Hair Removal System…
FDA device listing 1829640985 · Beijing Perfectlaser Technology Co.,Ltd
Key facts
| Proprietary names | Diode Laser Hair Removal System,Z820,Z860,Z840,Z870,Z890,,Long Pluse ND-YAG Alexandrite Laser Hair Removal System, Z110pro,Z110pro+,Z110Plus,Z110MAX,Z110MAX+ |
|---|---|
| Owner/operator | Beijing Perfectlaser Technology Co.,Ltd |
| Owner/operator number | 10085539 |
| Product codes | OHT |
| Device names | OHT - Light Based Over-The-Counter Hair Removal |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4810 |
| Review panels | General & Plastic Surgery |
| Registered establishments | BEIJING PERFECTLASER TECHNOLOGY CO.,LTD |
| Establishment registrations | 3023808190 |
| FEI numbers | 3023808190 |
| Establishment operations | Foreign Exporter, 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