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Aims: To validate cardiovascular risk prediction models for individuals with diabetes using the UK Biobank in order to assess their applicability. Methods: We externally validated 19 cardiovascular risk scores from seven risk prediction models (Chang et al., Framingham, University of Hong Kong‐Singapore [HKU‐SG], Li et al, RECODe [risk equations for complications of type 2 diabetes], SCORE [Systematic Coronary Risk Evaluation] and the UK Prospective Diabetes Study Outcomes Model 2 [UKPDS OM2]), identified from systematic reviews, using UK Biobank data from 2006 to 2021 (n = 23 685; participant age 40–71 years, 63.5% male). We evaluated performance by assessing the discrimination and calibration of the models for the endpoints of mortality, cardiovascular mortality, congestive heart failure, myocardial infarction, stroke, and ischaemic heart disease. Results: Over a total of 269 430 person‐years of follow‐up (median 11.89 years), the models showed low‐to‐moderate discrimination performance on external validation (concordance indices [c‐indices] 0.50–0.71). Most models had low calibration with overprediction of the observed risk. RECODe outperformed other models across four comparable endpoints for discrimination: all‐cause mortality (c‐index 0.67, 95% confidence interval [CI] 0.65–0.69), congestive heart failure (c‐index 0.71, 95% CI 0.69–0.72), myocardial infarction (c‐index 0.67, 95% CI 0.65–0.68); and stroke (c‐index 0.65, 95% CI 0.62–0.68), and for calibration (except for all‐cause mortality). The UKPDS OM2 had comparable performance to RECODe for all‐cause mortality (c‐index 0.67, 95% CI 0.66–0.69) and cardiovascular mortality (c‐index 0.71, 95% CI 0.70–0.73), but worse performance for other outcomes. The models performed better for younger participants and somewhat better for non‐White ethnicities. Models developed from non‐Western datasets showed worse performance in our UK‐based validation set. Conclusions: The RECODe model led to better risk estimations in this predominantly White European population. Further validation is needed in non‐Western populations to assess generalizability to other populations. [ABSTRACT FROM AUTHOR]