| aprevo | H.L61.02 | FDA UDI | Class II | Active |
| aprevo® | K.C34.03 | FDA UDI | Class II | Active |
| aprevo® | K.C56.03 | FDA UDI | Class II | Active |
| aprevo® | K.C78.03 | FDA UDI | Class II | Active |
| aprevo® | 1098.20.3 | FDA UDI | Class II | Active |
| aprevo® | 1251 | FDA UDI | Class II | Active |
| aprevo® | 1395 | FDA UDI | Class I | Active |
| aprevo | G.L34.02 | FDA UDI | Class II | Active |
| aprevo | J.L34.02 | FDA UDI | Class II | Active |
| aprevo | D.L61.03 | FDA UDI | Class II | Active |
| aprevo | G.L45.02 | FDA UDI | Class II | Active |
| aprevo | 1021 | FDA UDI | Class I | Active |
| aprevo | G.L34.03 | FDA UDI | Class II | Active |
| aprevo® | K.C34.02 | FDA UDI | Class II | Active |
| aprevo | C.L61.02 | FDA UDI | Class II | Active |
| aprevo | H.L51.02 | FDA UDI | Class II | Active |
| aprevo® anterior and lateral lumbar interbody system; aprevo® posterior and transforaminal lumbar interbody system; aprevo® cervical interbody system; corra™ cervical plating system | K260385 | FDA 510(k) | Class II | Active |
| aprevo Intervertebral Body Fusion Device | K202034 | FDA 510(k) | Class II | Active |
| aprevo® anterior and lateral lumbar interbody fusion device; aprevo® anterior lumbar interbody fusion devices with interfixation; aprevo® transforaminal lumbar interbody fusion device | K241332 | FDA 510(k) | Class II | Active |
| aprevo® posterior/transforaminal lumbar interbody fusion device | K250987 | FDA 510(k) | Class II | Active |
| aprevo® anterior lumbar interbody fusion device with interfixation | K243635 | FDA 510(k) | Class II | Active |
| aprevo® cervical plating system | K252611 | FDA 510(k) | Class II | Active |
| aprevo® cervical interbody system | K252894 | FDA 510(k) | Class II | Active |
| aprevo® Anterior and Lateral Lumbar Interbody Fusion device (ALIF/LLIF); aprevo® Transforaminal Lumbar Interbody Fusion device (TLIF); aprevo® Anterior Lumbar Interbody Fusion device with Interfixation (ALIF-X) | K241328 | FDA 510(k) | Class II | Active |
| aprevo® Digital Segmentation | K231955 | FDA 510(k) | Class II | Active |
| aprevo® transforaminal lumbar interbody fusion device | K231140 | FDA 510(k) | Class II | Active |
| aprevo® anterior lumbar interbody fusion device with interfixation | K222009 | FDA 510(k) | Class II | Active |
| aprevo® anterior and lateral lumbar interbody fusion devices, aprevo® transforaminal lumbar interbody fusion devices | K222082 | FDA 510(k) | Class II | Active |
| aprevo® Cervical ACDF; aprevo® Cervical ACDF-X; aprevo® Cervical ACDF-X NO CAM | K242260 | FDA 510(k) | Class II | Active |
| aprevo® anterior and lateral lumbar interbody fusion device, aprevo® anterior lumbar interbody fusion device with interfixation | K243802 | FDA 510(k) | Class II | Active |
| aprevo® Digital Planning | K242599 | FDA 510(k) | Class II | Active |
| aprevo® anterior lumbar interbody fusion device with interfixation | K241477 | FDA 510(k) | Class II | Active |
| aprevo® anterior lumbar interbody fusion device; aprevo® lateral lumbar interbody fusion device; aprevo® anterior lumbar interbody fusion device with interfixation; aprevo® transforaminal lumbar interbody fusion device; aprevo® TLIF-CA Articulating System; aprevo® Cervical ACDF; aprevo® Cervical ACDF-X; aprevo® Cervical ACDF-X No Cams | K250827 | FDA 510(k) | Class II | Active |
| aprevo Transforaminal IBF | K210542 | FDA 510(k) | Class II | Active |
| corra™ cervical plating system | K260570 | FDA 510(k) | Class II | Active |
| aprevo® TLIF-C Articulating System | K241019 | FDA 510(k) | Class II | Active |
| aprevo® anterior and lateral lumbar interbody fusion device, aprevo® transforaminal lumbar interbody fusion device | K232282 | FDA 510(k) | Class II | Active |
| aprevo® Digital Workflow | K222195 | FDA 510(k) | Class II | Active |