Jeisys Medical, Inc. - FDA 510(k) Cleared Devices

Jeisys Medical, Inc. has 15 FDA 510(k) cleared general & plastic surgery devices. Based in Littleton, US.

Latest FDA clearance: Dec 2024. Active since 2008.

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.

Regulatory submissions have been managed by LK Consulting Group USA, Inc., E & M and Iqvia.