| Taurus Pedicle Screw System | C | FDA UDI | Class II | Unknown |
| Taurus Pedicle Screw System | M | FDA UDI | Class II | Unknown |
| Taurus Pedicle Screw System | B | FDA UDI | Class II | Unknown |
| Taurus Pedicle Screw System | C | FDA UDI | Class II | Unknown |
| Taurus Pedicle Screw System | A | FDA UDI | Class II | Unknown |
| Valeo Cervical Plate System | K071990 | FDA 510(k) | Class II | Active |
| Valeo Pedicle Screw Spinal System | K072022 | FDA 510(k) | Class II | Active |
| Phantom Plus Ceramic Cage System | K121892 | FDA 510(k) | Class II | Active |
| Modification To Valeo Vbr | K073505 | FDA 510(k) | Class II | Active |
| Amedica Valeo II Interbody Fusion Device | K142347 | FDA 510(k) | Class II | Active |
| Valeo® C+CSC with Lumen Interbody Fusion Device | K173453 | FDA 510(k) | Class II | Active |
| Seeplate Cervical Plate System | K082037 | FDA 510(k) | Class II | Active |
| Arx Spinal System | K051525 | FDA 510(k) | Class II | Active |
| Valeo Spacer System and Valeo II Interbody Fusion Device System | K143518 | FDA 510(k) | Class II | Active |
| Valeo C Spacer System, Valeo II C IBF Device | K142264 | FDA 510(k) | Class II | Active |
| Preference Elite Pedicle Screw System | K162160 | FDA 510(k) | Class II | Active |
| Valeo Vbr | K073125 | FDA 510(k) | Class II | Active |
| Vented Cement Restrictor | K022729 | FDA 510(k) | Class II | Active |
| Modification To: Vented Cement Restrictor, Model 60102-000-001/004 | K050699 | FDA 510(k) | Class II | Active |
| Valeo Spacer System | K091278 | FDA 510(k) | Class II | Active |
| Valeo II Interbody Fusion Device System | K161405 | FDA 510(k) | Class II | Active |
| Valeo Pedicle Screw Spinal System | K073430 | FDA 510(k) | Class II | Active |