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COMPANY

Life Spine

HQ: Huntley, IL source · lifespine.com ↗ · Midwest

FDA-cleared device company

Location: Huntley, IL · source · Oct 14, 2026

Profile checked Oct 10, 2026

9FDA records (2 yrs)

Timeline

  1. FDA FDA 510(k) clearance: TruLift Expandable System — K261430, Jul 28, 2026. Applicant at approval: Life Spine, Inc. source ↗
  2. FDA FDA 510(k) clearance: SIMPACT Sacroiliac Joint Fixation System GX Navigation Instruments — K260571, Jun 2, 2026. Applicant at approval: Life Spine, Inc. source ↗
  3. FDA FDA 510(k) clearance: VersaLift Expandable System — K260837, May 12, 2026. Applicant at approval: Life Spine, Inc. source ↗
  4. FDA FDA 510(k) clearance: ARx® SAI Implant System — K254274, Apr 16, 2026. Applicant at approval: Life Spine, Inc. source ↗
  5. FDA FDA 510(k) clearance: Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System — K253748, Jan 23, 2026. Applicant at approval: Life Spine, Inc. source ↗
  6. FDA FDA 510(k) clearance: TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System — K251502, Jul 7, 2025. Applicant at approval: Life Spine, Inc. source ↗
  7. FDA FDA 510(k) clearance: ProLift Expandable Spacer System — K250373, Apr 9, 2025. Applicant at approval: Life Spine, Inc. source ↗
  8. FDA FDA 510(k) clearance: ProLift Pivot Expandable Spacer System — K243668, Jan 23, 2025. Applicant at approval: Life Spine, Inc. source ↗
  9. FDA FDA 510(k) clearance: Cervical Plating System — K243369, Dec 11, 2024. Applicant at approval: Life Spine, Inc. source ↗

FDA records (last 2 years)

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LinkedIn page linked from the company's own site: source · seen 2026-10-12

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