Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System

Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System is an FDA 510(k)-cleared medical device (K253748) manufactured by Life Spine, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 22, 2026. Regulation: 8.