The synergistic fusion of photoredox catalysis and transition-metal catalysis denominated metallaphotoredox reaction. Over the past decades, the merging of metal catalysis and photoredox catalysis has surfaced as a diverse and powerful technique in the production of challenging molecular synthesis. The vast dominance of photoredox concepts exploits heavy, precious and expensive metals. Iridium or ruthenium-based complexes obey single-electron reductants or oxidants in their photoexcited states. Thus, copper-based photocatalysts have rapidly sprung up in photochemistry due to their non-toxicity, abundance, low price, and novel properties, including inner coordination sphere mechanisms. Nevertheless, they exhibit tunable redox characteristics in their excited states, allowing stereoinduction accommodating flexible ligand architecture. Multiple accessible oxidation states are being accomplished for facile reductive elimination, oxidative addition, rapid radical capture and C?C/ C?N/ C?O/ C?S/ C?X cross-coupling reactions. We notice that there are plenty of research done on the concept of synergistic fusion of photo-redox and copper catalysis. Specifically, on this account we describe the latest advancements in light-mediated merged copper-photoredox catalysis as initiation in organic transformations, focusing on substrate scope, limitations, mechanistic paradigms, and various applications. This review covers the literature from 2018 to 2024.