FDA device listing
CurrentBody LED Light Therapy Mask: Series 3,CurrentBody Skin LED Multi Light Therapy Mask
FDA device listing 1910215036 · Currentbody Ltd.
Key facts
| Proprietary names | CurrentBody LED Light Therapy Mask: Series 3,CurrentBody Skin LED Multi Light Therapy Mask |
|---|---|
| Owner/operator | Currentbody Ltd. |
| Owner/operator number | 10060586 |
| Premarket submissions | K260715 |
| Product codes | OHS, OLP |
| Device names | OHS - Light Based Over The Counter Wrinkle Reduction, OLP - Over-The-Counter Powered Light Based Laser For Acne |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4810 |
| Review panels | General & Plastic Surgery |
| Registered establishments | The Beauty Tech Group Ltd |
| Establishment registrations | 3014737458 |
| FEI numbers | 3014737458 |
| Establishment operations | Foreign Exporter, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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