Topcon Corporation - FDA 510(k) Cleared Devices

Topcon Corporation has 13 FDA 510(k) cleared ophthalmic devices. Based in North Reading, US.

Latest FDA clearance: Nov 2025. Active since 2014.

Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Orasi Consulting, Oconnell Regulatory Consultants, Inc. and Orasi Consulting, LLC. 1 device has linked clinical trial registered on ClinicalTrials.gov.