Inmode MD , Ltd. - FDA 510(k) Cleared Devices

Inmode MD , Ltd. has 21 FDA 510(k) cleared general & plastic surgery devices. Based in Kfar Saba, IL.

Last cleared in 2021. Active since 2013.

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

510(k) submissions have been managed by A. Stein - Regulatory Affairs Consulting , Ltd. as regulatory consultant.