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

Mnlase, Inc. has 22 FDA 510(k) cleared general & plastic surgery devices. Based in Minneapolis, US.

Historical record: 22 cleared submissions from 1992 to 1994.

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.