Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Expanding Innovations with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jun 25, 2025: X-PAC® LLIF Expandable Lateral Cage 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.
| Jun 25, 2025 | X-PAC® LLIF Expandable Lateral Cage SystemK251003 · MAX | 510(k) clearances |
| Jun 16, 2025 | X-PAC® TLIF Expandable Posterior Cage System; X-PAC® LLIF Expandable Lateral Cage SystemK251617 · MAX | 510(k) clearances |
| May 20, 2025 | X-PAC® N-GAGE™ Lumbar Plate SystemK250602 · KWQ | 510(k) clearances |
| Feb 14, 2023 | X-Pac Expandable LLIF Cage SystemK223174 · MAX | 510(k) clearances |
| Oct 14, 2022 | X-Pac Expandable Lumbar Cage SystemK222797 · MAX | 510(k) clearances |
| Mar 24, 2022 | X-Pac Expandable Lumbar Cage SystemK220655 · MAX | 510(k) clearances |
| Jun 7, 2021 | X-Pac Expandable Lumbar Cage SystemK203802 · MAX | 510(k) clearances |
| Sep 10, 2020 | X-Pac Expandable Lumbar Cage SystemK201145 · 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
