Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Life Spine with 123 510(k) clearances. The most recent is a 510(k) clearance dated Jul 28, 2026: TruLift Expandable System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jul 28, 2026 | TruLift Expandable SystemK261430 · MAX | 510(k) clearances |
| Jun 2, 2026 | SIMPACT Sacroiliac Joint Fixation System GX Navigation InstrumentsK260571 · OLO | 510(k) clearances |
| May 12, 2026 | VersaLift Expandable SystemK260837 · MAX | 510(k) clearances |
| Apr 16, 2026 | ARx® SAI Implant SystemK254274 · NKB | 510(k) clearances |
| Jan 23, 2026 | Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer SystemK253748 · MAX | 510(k) clearances |
| Jul 7, 2025 | TruLift® Lateral Expandable Spacer & Lateral Buttress Plate SystemK251502 · MAX | 510(k) clearances |
| Apr 9, 2025 | ProLift Expandable Spacer SystemK250373 · MAX | 510(k) clearances |
| Jan 23, 2025 | ProLift Pivot Expandable Spacer SystemK243668 · MAX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
