FDA 510(k) Applications Submitted by Luminopia, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K233720 11/21/2023 Luminopia Luminopia, Inc.
DEN210005 03/01/2021 Luminopia One Luminopia, Inc.
K221659 06/08/2022 Luminopia One Luminopia, Inc.
K243819 12/12/2024 Luminopia Luminopia, Inc.


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