Vacuum‐based deposition of halide perovskites has received a lot of attention for its proven scalability and conformal depositions. Co‐evaporation has had remarkable success, but efficiencies continue to lag behind their solution‐based counterparts. This is in part attributed to the complex sublimation behavior of some organic ammonium precursor salts and the increased complexity of the absorber materials, requiring the use of four or more sources in a conventional co‐evaporation setup. The latter has driven work into single‐source methods with flash evaporation presented as one such method. However, flash evaporation processes typically evaporate all material in a single batch, leading to short deposition times at high temperatures. Particle sputtering effects seen at these high temperatures drive processes towards low temperatures where prolonged exposure causes degradation. Here, we present a pulse‐driven incremental powder feeding system. This method is capable of stable flash evaporation rates for >1 hour, with controlled rates as low as 1.5 Å per pulse (+‐ 0.89). We demonstrate the feasibility of this method for three different perovskite compositions: FAPbBr3, MAPbI3, and FA1‐xMAxPbSnI3:SnF2. Furthermore, we integrate FAPbBr3 and MAPbI3 into all vacuum‐processed thin‐film solar cells leading to power conversion efficiencies of ∽4% and 10% respectively.This article is protected by copyright. All rights reserved.