Ocuject, LLC - FDA 510(k) Cleared Devices

Ocuject, LLC has 8 FDA 510(k) cleared medical devices. Based in Newport Beach, US.

Latest FDA clearance: Oct 2024. Active since 2017. Primary specialty: General Hospital.

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

Regulatory submissions have been managed by Namsa and Regulatory Resources Group, Inc..