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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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