| ARIA Radiation Therapy Management (v18.0) | K230699 | FDA 510(k) | Class II | Active |
| 4D Integrated Treatment Console | K203766 | FDA 510(k) | Class II | Active |
| Anchored Beacon(R) transponder, Anchored transponder, Beacon Care Package - Lung | K170570 | FDA 510(k) | Class II | Active |
| Modification To: On-Board Imager Device | K041519 | FDA 510(k) | Class II | Active |
| Treatvision | K002194 | FDA 510(k) | Class II | Active |
| Modification To Eclipse Treatment Planning System | K071873 | FDA 510(k) | Class II | Active |
| Unique | K132705 | FDA 510(k) | Class II | Active |
| Acuity With Conebeam Computed Tomography | K033339 | FDA 510(k) | Class II | Active |
| Halcyon, Ethos Radiotherapy System | K232113 | FDA 510(k) | Class II | Active |
| Varian Multileaf Collimator | K133240 | FDA 510(k) | Class II | Active |
| Trilogy Radiotherapy Delivery System And Trilogy Tx Delivery System | K070094 | FDA 510(k) | Class II | Active |
| Varian Cleaning Caps, Varian Leak Stop Buttons, Varian Leak Stop Channel Marker Sets | K152018 | FDA 510(k) | Class II | Active |
| Vision | K042956 | FDA 510(k) | Class II | Active |
| TrueBeam, TrueBeam STx, EDGE and VitalBeam (4.1) | K232870 | FDA 510(k) | Class II | Active |
| Varian Treatment (VTx) | K151882 | FDA 510(k) | Class II | Active |
| 3D Interstitial Ring Applicator Set 60, 3D Interstitial Ring Applicator Set 90, Ring Applicator Set 45, Ring Applicator Set 60, Ring Applicator Set 90 | K150839 | FDA 510(k) | Class II | Active |
| Smart Segmentation Knowledge Based Contouring | K141248 | FDA 510(k) | Class II | Active |
| High Energy Linear Accelerator | K131807 | FDA 510(k) | Class II | Active |
| Shielded Applicator Set, Cervical Stop | K151657 | FDA 510(k) | Class II | Active |
| ProBeam 360° Proton Therapy System v2.0 (Multiroom) | K231863 | FDA 510(k) | Class II | Active |
| TrueBeam, TrueBeam STx, Edge, VitalBeam | K213977 | FDA 510(k) | Class II | Active |
| Embozene Color-Advanced Microspheres | K242608 | FDA 510(k) | Class II | Active |
| TrueBeam, TrueBeam STX, Edge and VitalBeam | K252948 | FDA 510(k) | Class II | Active |
| On-Board Imager Device | K040192 | FDA 510(k) | Class II | Active |
| Standard Catheter Set | K171631 | FDA 510(k) | Class II | Active |
| ProBeam 360 Proton Therapy System v3.0 | K252815 | FDA 510(k) | Class II | Active |
| Universal Segmented Cylinder Applicator Set And Universal Stump Applicator Set | K141490 | FDA 510(k) | Class II | Active |
| Universal Cylinder Applicator Family, Universal Segmented Cylinder Applicator Set, Universal Stump Applicator Set, Universal Cervix Probe Set, odd lengths, Universal Cervix Probe Set, even lengths | K160516 | FDA 510(k) | Class II | Active |
| Esophagus Bougie Set | K161576 | FDA 510(k) | Class II | Active |
| Trilogy System With Rapidarc | K072916 | FDA 510(k) | Class II | Active |
| Kelowna GYN and Crook Prostate Templates | K232949 | FDA 510(k) | Class II | Active |
| Rpm Respiratory Gating System | K983629 | FDA 510(k) | Class II | Active |
| Universal Cylinder Applicator Family, Universal Segmented Cylinder Applicator Set, Universal Stump Applicator Set, Universal Cervix Probe Sets, odd lengths and even lengths, Universal Titanium Cervix Probe Sets, odd lengths and even lengths | K172611 | FDA 510(k) | Class II | Active |
| 4d Integrated Treatment Console With Patient Accessory Verification System (pavs) | K081036 | FDA 510(k) | Class II | Active |
| Portalvision | K003636 | FDA 510(k) | Class II | Active |
| Urethral Warming Catheter Kit | K211149 | EUDAMEDFDA 510(k)FDA UDI | Class II | Active |
| Eclipse, Helios Option | K021268 | FDA 510(k) | Class II | Active |
| Mould Applicator Set | K162615 | FDA 510(k) | Class II | Active |
| Eclipse Treatment Planning System (v18.0) | K230557 | EUDAMEDFDA 510(k)FDA UDI | Class II | Active |
| Eclipse Treatment Planning System v16.1 | K201607 | FDA 510(k) | Class II | Active |
| GM Implant Tubes, Length Cutting Gauge | K172533 | FDA 510(k) | Class II | Active |
| syngo.via RT Image Suite VC10 | K252304 | FDA 510(k) | Class II | Active |
| TrueBeam-TrueBeam STx-Edge | K143224 | FDA 510(k) | Class II | Active |
| Varian Nasopharynx Applicator | K042360 | FDA 510(k) | Class II | Active |
| TrueBeam, TrueBeam STx, Edge | K171733 | FDA 510(k) | Class II | Active |
| Permanent Beacon Transponder, Soft Tissue Beacon Transponder, Beacon Care Package - Soft Tissue (17G) | K152761 | FDA 510(k) | Class II | Active |
| Acuity Radiation Therapy Simulator | K023052 | FDA 510(k) | Class II | Active |
| Trilogy Mx | K092871 | FDA 510(k) | Class II | Active |
| Halcyon, Ethos Radiotherapy System | K222941 | FDA 510(k) | Class II | Active |
| TrueBeam, TrueBeam STx, Edge, VitalBeam | K231317 | FDA 510(k) | Class II | Active |