Hydrogels are important functional materials useful for 3D cell culture, tissue engineering, 3D printing, drug delivery, sensors, or soft robotics. The ability to shape hydrogels into defined 3D structures, patterns, or particles is crucial for biomedical applications. Here, the rapid photodegradability of commonly used polymethacrylate hydrogels is demonstrated without the need to incorporate additional photolabile functionalities. Hydrogel degradation depths are quantified with respect to the irradiation time, light intensity, and chemical composition. It can be shown that these parameters can be utilized to control the photodegradation behavior of polymethacrylate hydrogels. The photodegradation kinetics, the change in mechanical properties of polymethacrylate hydrogels upon UV irradiation, as well as the photodegradation products are investigated. This approach is then exploited for microstructuring and patterning of hydrogels including hydrogel gradients as well as for the formation of hydrogel particles and hydrogel arrays of welldefined shapes. Cell repellent but biocompatible hydrogel microwells are fabricated using this method and used to form arrays of cell spheroids. As this method is based on readily available and commonly used methacrylates and can be conducted using cheap UV light sources, it has vast potential to be applied by laboratories with various backgrounds and for diverse applications.various applications in biotechnological and biomedical fields, including actuators, [2] sensors, [3] artificial muscles, [4] drug delivery, [1a] and tissue engineering. [5] These and many other applications require hydrogels with well-defined chemical and physical properties, shape, topography, mechanical properties, porosity and biocompatibility. [6] Several types of photodegradable hydrogels have been introduced in literature to prepare microstructured soft materials or to define chemical and physical properties with spatiotemporal control. [7] However, to achieve hydrogel photodegradability, artificial photoresponsive units or crosslinkers had to be synthesized and incorporated into the hydrogel network, which would then serve as breaking points under UV light. Such photodegradable moieties include o-nitrobenzyl ester, [8] coumarins, [9] disulfides, [10] Ru II polypyridyl complexes, [11] etc. The limited number of available photolabile groups and the need for their synthesis and incorporation into the hydrogel network significantly limit the number and scope of possible applications of photodegradable hydrogels for a broader audience. Here we demonstrate, for the first time, that one of the most commonly used types of hydrogels, i.e., hydrogels based on hydrophilic polymethacrylates, can be efficiently degraded using UV light without requiring any external photolabile moieties ( Figure 1A). The different