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/ Luminopia, Inc.
Luminopia, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K243819
Luminopia
April 9, 2025
K233720
Luminopia
August 8, 2024
K221659
Luminopia One
November 4, 2022
DEN210005
Luminopia One
October 20, 2021