SPINAL MARKER
Apr 1995
230d
Leibinger L.P. has 1 FDA 510(k) cleared medical devices. Based in Dallas, US.
Historical record: 1 cleared submissions from 1995 to 1995. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Leibinger L.P. Filter by specialty or product code using the sidebar.