FDA device listing
BRIGHT SPOT I,BRIGHT SPOT II,BRIGHT SPOT III,BRIGHT SPOT IV,BRIGHT SPOT V,BRIGHT SPOT VI,TENDER SPOT
FDA device listing 1656549170 · GEORGE TAUB PRODUCTS & FUSION CO., INC.
Key facts
| Proprietary names | BRIGHT SPOT I,BRIGHT SPOT II,BRIGHT SPOT III,BRIGHT SPOT IV,BRIGHT SPOT V,BRIGHT SPOT VI,TENDER SPOT |
|---|---|
| Owner/operator | GEORGE TAUB PRODUCTS & FUSION CO., INC. |
| Owner/operator number | 2241860 |
| Product codes | EFH |
| Device names | EFH - Paper, Articulation |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.6140 |
| Review panels | Dental |
| Registered establishments | GEORGE TAUB PRODUCTS & FUSION CO., INC. |
| Establishment registrations | 2241860 |
| FEI numbers | 2241860 |
| 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