FDA device listing
Greater Curve Large Brass Sectional Matrix,Greater Curve Micro Thin matrix bands,Greater Curve Micro U-Band matrix…
FDA device listing 1839412884 · Greater Curve
Key facts
| Proprietary names | Greater Curve Large Brass Sectional Matrix,Greater Curve Micro Thin matrix bands,Greater Curve Micro U-Band matrix bands,Greater Curve Micro Wide matrix bands,Greater Curve Small Brass Sectional Matrix,Greater Curve Standard Brass matrix bands,Greater Curve Standard matrix bands,Greater Curve U-Band Brass matrix bands,Greater Curve U-Band matrix bands,Greater Curve Wide Brass matrix bands,Greater… |
|---|---|
| Owner/operator | Greater Curve |
| Owner/operator number | 10082825 |
| Product codes | EKF |
| Device names | EKF - Instrument, Contouring, Matrix, Operative |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.4565 |
| Review panels | Dental |
| Registered establishments | GREATER CURVE |
| Establishment registrations | 3020650140 |
| FEI numbers | 3020650140 |
| Establishment operations | Repackager/Relabeler, 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