Meris Investment Group - FDA 510(k) Cleared Devices

Meris Investment Group has 2 FDA 510(k) cleared medical devices. Based in Lakeland, US.

Last cleared in 2023. Active since 2021. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Meris Investment Group Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Prime Path Medtech and Medavice, Inc..