FDA device listing
Patient Relief Wax
FDA device listing 1104634117 · LIBRAL TRADERS PVT. LTD.
Key facts
| Proprietary names | Patient Relief Wax |
|---|---|
| Owner/operator | LIBRAL TRADERS PVT. LTD. |
| Owner/operator number | 10085246 |
| Product codes | EGD |
| Device names | EGD - Wax, Dental, Intraoral |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.6890 |
| Review panels | Dental |
| Registered establishments | LIBRAL TRADERS PVT. LTD. |
| Establishment registrations | 3009268271 |
| FEI numbers | 3009268271 |
| 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