FDA device listing
Restoration, resin, crown and bridge
FDA device listing 1691061835 · Promax Dental Laboratory Limited
Key facts
| Proprietary names | Restoration, resin, crown and bridge |
|---|---|
| Owner/operator | Promax Dental Laboratory Limited |
| Owner/operator number | 10059281 |
| Product codes | NSN |
| Device names | NSN - Restoration, Resin, Crown And Bridge |
| Device class | Not classified |
| Classification regulations (21 CFR) | ORCA1.NSN |
| Review panels | Dental |
| Registered establishments | PROMAX DENTAL LABORATORY LIMITED |
| Establishment registrations | 3014736129 |
| FEI numbers | 3014736129 |
| Establishment operations | Foreign Exporter |
| 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