FDA device listing
WE Light Class II
FDA device listing 1065050085 · WHITE ESSENCE CO.,LTD.
Key facts
| Proprietary names | WE Light Class II |
|---|---|
| Owner/operator | WHITE ESSENCE CO.,LTD. |
| Owner/operator number | 10090949 |
| Product codes | EEG |
| Device names | EEG - Heat Source For Bleaching Teeth |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.6475 |
| Review panels | Dental |
| Registered establishments | WHITE ESSENCE Co., Ltd |
| Establishment registrations | 3030670291 |
| FEI numbers | 3030670291 |
| Establishment operations | Specification Developer |
| 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