Medical Device Manufacturer · US , Cambridge , MA

Luminopia, Inc. - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 2021

Total

Cleared

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.

FDA 510(k) cleared devices by Luminopia, Inc.

4 devices

1-4 of 4