Life Spine revealed that its ProLift expandable interbody portfolio was evaluated and confirmed as MR conditional in accordance with ASTM standards.

This newly granted MR Conditional status includes ProLift, ProLift Micro, and ProLift Lateral. These devices are designed to support interbody fusion procedures in TLIF, PLIF, and LLIF. The designation means that patients implanted with the devices can safely have MRI scans under specific conditions, which are outlined in product labeling.

MRI safety designation is crucial for modern spine care because post-op imaging is extremely important in patient monitoring and long-term clinical management.

The evaluation of Life Spine’s interbodies included assessment of magnetic field interactions, heating, and image artifacts in accordance with recognized industry standards. Specific scanning parameters and conditions are soon to be available in the product Instructions for Use (IFU), the company said.

“Our team is committed to ensuring our technologies meet the evolving needs of both surgeons and patients,” said Rich Mueller, CEO at Life Spine. “The confirmation of MR Conditional status reflects our continued commitment to developing carefully engineered solutions that support both procedural efficiency and long-term patient monitoring.”

In November, Life Spine voluntarily dismissed its lawsuit against founder and CEO Michael Butler. This follows a court ruling that dismissed the majority of the company’s claims before discovery even began.