Luminopia, Inc. - FDA 510(k) Cleared Devices
4
Total
3
Cleared
1
Denied
Luminopia, Inc. has 3 FDA 510(k) cleared medical devices. Based in Cambridge, US.
Latest FDA clearance: Apr 2025. Active since 2021. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Luminopia, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
4 devices