Life Spine, Inc. - FDA 510(k) Cleared Devices

Life Spine, Inc. is a spinal medical device company headquartered in Huntley, Illinois. Founded in 2004, the company develops innovative solutions for spinal pathology across the cervical, thoracic, and lumbar spine. Life Spine serves 32 countries and employs over 70 people worldwide.

The company has received 84 FDA 510(k) clearances from 84 total submissions since 2011. Life Spine specializes exclusively in Orthopedic devices, with a focus on minimally invasive spinal fusion solutions. The latest clearance was in 2026, confirming active regulatory engagement.

Life Spine's product portfolio centers on expandable interbody spacer systems, spinal fixation implants, and biologics for fusion procedures. Key product lines include the ProLift expandable spacer family, TruLift lateral expandable systems, and ARx sacroiliac joint fixation implants. The company also offers cervical plating systems and minimally invasive spinal screw solutions.

Explore the complete list of cleared device names, product codes, and clearance dates in the database.