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

Moleculight, Inc. has 4 FDA 510(k) cleared medical devices. Based in Toronto, CA.

Last cleared in 2022. Active since 2018. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Ironstone Product Development as regulatory consultant. 3 devices have linked clinical trials registered on ClinicalTrials.gov.