FDA device listing
NovoTHOR,NovoTHOR Standard,NOVOTHOR Whole Body Light Pod,NovoTHOR XL Whole Body Light Pod
FDA device listing 1582664559 · THOR Photomedicine Ltd
Key facts
| Proprietary names | NovoTHOR,NovoTHOR Standard,NOVOTHOR Whole Body Light Pod,NovoTHOR XL Whole Body Light Pod |
|---|---|
| Owner/operator | THOR Photomedicine Ltd |
| Owner/operator number | 9054807 |
| Product codes | ILY |
| Device names | ILY - Lamp, Infrared, Therapeutic Heating |
| Device class | Class II |
| Classification regulations (21 CFR) | 890.5500 |
| Review panels | Physical Medicine |
| Registered establishments | THOR PHOTOMEDICINE INC., THOR Photomedicine Ltd |
| Establishment registrations | 3003899624, 3034745472 |
| FEI numbers | 3003899624, 3034745472 |
| Establishment operations | Manufacturer, 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