FDA device listing
PRISM LIGHT POD 4th Generation
FDA device listing 1359360551 · Prism Light Pod
Key facts
| Proprietary names | PRISM LIGHT POD 4th Generation |
|---|---|
| Owner/operator | Prism Light Pod |
| Owner/operator number | 10083396 |
| 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 | PRISM LIGHT POD |
| Establishment registrations | 3020954225 |
| FEI numbers | 3020954225 |
| 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