Visual processing mainly occurs during fixation, periods separated by saccadic eye movements, necessitating a close coordination between sensory and motor systems. It has been suggested that the intention to make a saccade can modulate neural activity, including predictive changes, suppression of peri-saccadic retinal input and trans-saccadic integration. Consistent with this idea, modulations of neural activity around the time of saccades have been reported in non-human species, showing non-visually mediated, extraretinal responses in specific brain regions. In humans, however, peri-saccadic whole-brain activity has mainly been studied in the context of a perceptual task, making it difficult to disentangle activity related to the task, visual transients from retinal stimulation and non-visual (saccade-related) responses. We measured magnetoencephalography (MEG) theta (3–7 Hz) and alpha (8–12 Hz) activity during voluntary horizontal saccade execution between two fixation points. To distinguish between visually and non-visually mediated activity, participants engaged in three tasks: voluntary saccades in near-darkness, fixation with visual input shifted to simulate the saccade, and volitional saccades in total darkness. Using correlational analyses, we found that patterns of neural activity are consistent with contributions of two separate mechanisms, one related to saccades (non-visual/extraretinal) and the other linked to the processing of visual input at the beginning of the new fixation (visual/retinal). Changes in occipital alpha power and instantaneous frequency showed a similar time course in near-dark and simulated saccade conditions, suggesting an effect of visually evoked responses. In contrast, alterations in parietal-occipital theta power and phase clustering were consistent with a non-visually-driven (extraretinal) mechanism, with similar multivariate patterns for near-dark and full-darkness conditions. Some effects, such as theta phase reset and alterations in alpha power, showed separable contributions of both the saccade and visual transient, with differing time courses. This combination of visual and non-visual mechanisms may support sensorimotor integration during active vision.