In　this　study,　a　visible-light-mediated　two-component　beta-fluoro-fluorosulfonamidation　reaction　of　styrenes　is　demonstrated.　The　bench-stable　reagent,　N-fluorosulfamoyl-pyridinium　tetrafluoroborate　can　be　used　as　a　photoredox-active　nitrogen-centered　radical　precursor　and　also　as　the　fluoride　source.　This　transformation　can　convert　a　series　of　styrenes　to　functional　group-enriched　products,　including　substrates　with　electron-donating　or　withdrawing　groups,　as　well　as　di-　and　tri-substituents　on　the　C-C　double　bond.