FDA 510(k) Applications Submitted by Aesthetic Technology Ltd

FDA 510(k) Number Submission Date Device Name Applicant
K202028 07/22/2020 dermalux Flex MD Aesthetic Technology Ltd
K240222 01/26/2024 Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024) Aesthetic Technology Ltd


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