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PURPOSE: The purpose of this study is to validate the iHealth-BP7 and Withings-BP800 monitors according to the European Society of Hypertension (ESH) International Protocol revision 2010. METHODS: Data from 11 participants (31.6 ± 2.2 years) were initially examined according to the ESH International Protocol for the validation of BP measuring devices. Participants were asked to sit and relax for 10-15 mins with legs uncrossed, and back supported prior to the test. In all participants, sequential left arm measurements were performed by two trained observers using a mercury sphygmomanometer and one supervisor using the device. Collected data were screened according to the ESH protocol RESULTS: The mean differences between the monitor and sphygmomanometer readings were -0.55±3.75 (SBP) and 0.54±3.62 (DBP) for iHealth-BP7 and 3.18±4.37 (SBP) and - 0.35±5.42 (DBP) for Withings-BP800. The iHealth-BP7 monitor passed all of the modified requirements, however the WithingsBP800 did not meet the last phase of the modified protocol. CONCLUSION: The iHealth-BP7 monitor is recommended as a valid home BP monitoring device, however the Withings-BP800 fails to meet the ESH criteria in this study potentially due to the small sample size. Since the ESH protocol requires 33 subjects, further study with additional participants is warranted to determine validation of both devices.