FDA device listing
CarboClear® Cervical Cage System,CarboClear® Cervical VBR System
FDA device listing 2013750857 · CarboFix Orthopedics Ltd.
Key facts
| Proprietary names | CarboClear® Cervical Cage System,CarboClear® Cervical VBR System |
|---|---|
| Owner/operator | CarboFix Orthopedics Ltd. |
| Owner/operator number | 10035372 |
| Premarket submissions | K222874 |
| Product codes | ODP, PLR |
| Device names | ODP - Intervertebral Fusion Device With Bone Graft, Cervical, PLR - Spinal Vertebral Body Replacement Device - Cervical |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3060, 888.3080 |
| Review panels | Orthopedic |
| Registered establishments | CarboFix Orthopedics, Ltd. |
| Establishment registrations | 9615128 |
| FEI numbers | 3008820440 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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