C. Light Technologies, Inc. - FDA 510(k) Cleared Devices

C. Light Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Medford, US.

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

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

510(k) submissions have been managed by Blur Product Development as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.