FDA device listing
CD-0206,CD-0208,CD-0210 CD-0211 CD-0213 CD-0216 CD-2806 CD-2808 CD-2810 CD-2811 CD-2813 CD-2816,CD-1001 CD-5003 CD-5010…
FDA device listing 1298450020 · Cortex Dental Implants Industries Ltd.
Key facts
| Proprietary names | CD-0206,CD-0208,CD-0210 CD-0211 CD-0213 CD-0216 CD-2806 CD-2808 CD-2810 CD-2811 CD-2813 CD-2816,CD-1001 CD-5003 CD-5010 CD-5020 CD-5025 CD-5030 CD-5040 CD-5045 CD-5050 CD-5060,CD-3206 CD-3208 CD-3210 CD-3211 CD-3213 CD-3706 CD-3708 CD-3710 CD-3711 CD-3713,CD-4306 CD-4308 CD-4310 CD-4311 CD-4313 CD-GS0822 CD-GS0828 CD-GS0834 CD-GS0837 CD-GS0841,CD-5065 CD-5110 CD-5120 CD-5140 CD-5148 CD-5137… |
|---|---|
| Owner/operator | Cortex Dental Implants Industries Ltd. |
| Owner/operator number | 10030174 |
| Product codes | DZA |
| Device names | DZA - Drill, Dental, Intraoral |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.4130 |
| Review panels | Dental |
| Registered establishments | CORTEX DENTAL IMPLANTS INDUSTRIES LTD. |
| Establishment registrations | 3007842672 |
| FEI numbers | 3007842672 |
| 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