| PERLA® TL Posterior Osteosynthesis System | K213470 | FDA 510(k) | Class II | Active |
| Romeo Posterior Osteosynthesis System | K130267 | FDA 510(k) | Class II | Active |
| Ellipse Lumbar Posterior Osteosynthesis System | K081165 | FDA 510(k) | Class II | Active |
| Perla Posterior Cervico-Thoracic Fixation system | K153386 | FDA 510(k) | Class II | Active |
| SPINEART Navigation Instrument System | K241644 | FDA 510(k) | Class II | Active |
| Tryptik Ca Anterior Intersomatic Cervical Cage, Models Mos-Ca 12 05-S, Mos-Ca 12 O6-S | K091873 | FDA 510(k) | Class II | Active |
| SPINEART Navigation Instrument System | K183630 | FDA 510(k) | Class II | Active |
| Tryptik Ti | K230583 | FDA 510(k) | Class II | Active |
| ROMEO® 2 Posterior Osteosynthesis System | K172101 | FDA 510(k) | Class II | Active |
| Romeo Posterior Osteosynthesis System | K093936 | FDA 510(k) | Class II | Active |
| SCARLET® AC-T Secured Anterior Cervical Cage | K143214 | FDA 510(k) | Class II | Active |
| SCARLET® AC-T Secured Anterior Cervical Cage | K190322 | FDA 510(k) | Class II | Active |
| Juliet® Ti LL Lumbar Interbody Device | K190877 | FDA 510(k) | Class II | Active |
| Dynamik Intervertebral Body Fusion Device | K081888 | FDA 510(k) | Class II | Active |
| Scarlet® AL-T | K242589 | FDA 510(k) | Class II | Active |
| PERLA® Posterior Occipito-Cervico-Thoracic Fixation System | K200571 | FDA 510(k) | Class II | Active |
| Juliet Ll Lateral Lumbar Cage | K133557 | FDA 510(k) | Class II | Active |
| Juliet Ti | K181203 | FDA 510(k) | Class II | Active |
| Juliet Po | K142277 | FDA 510(k) | Class II | Active |
| Romeo Posterior Osteosynthesis System | K112108 | FDA 510(k) | Class II | Active |
| Romeo Posterior Osteosynthesis System | K093170 | FDA 510(k) | Class II | Active |
| Perla® Posterior Cervico-Thoracic Fixation System | K190071 | FDA 510(k) | Class II | Active |
| Tryptik Cc Anterior Intersomatic Cervical Cage | K122366 | FDA 510(k) | Class II | Active |
| SCARLET® AC-Ti | K240699 | FDA 510(k) | Class II | Active |
| TRYPTIK2 C-Plate Anterior Cervical Plate System | K171797 | FDA 510(k) | Class II | Active |
| Juliet Ol | K140474 | FDA 510(k) | Class II | Active |
| Juliet Ll | K141135 | FDA 510(k) | Class II | Active |
| Juliet Ol | K101720 | FDA 510(k) | Class II | Active |
| Romeo Posterior Osteosynthesis System Prebent Cross-Connectors; Prebent Rods | K141835 | FDA 510(k) | Class II | Active |
| PERLA® TL System; TEKTONA® HV US Bone Cement | K230774 | FDA 510(k) | Class II | Active |
| Romeo 2 Pad Posterior Axial Device | K141508 | FDA 510(k) | Class II | Active |
| SPINEART Navigation Instrument System | K242890 | FDA 510(k) | Class II | Active |
| SPINEART Navigation Instrument System | K242933 | FDA 510(k) | Class II | Active |
| Tryptik Ti | K200312 | FDA 510(k) | Class II | Active |