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

Acculens, Inc. has 1 FDA 510(k) cleared medical devices. Based in Lakewood, US.

Last cleared in 2023. Active since 2023. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Acculens, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Eyereg Consulting, Inc. as regulatory consultant.