Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Nexus Spine, LLC with 19 510(k) clearances. The most recent is a 510(k) clearance dated Jun 22, 2026: DeltaNEC Interbody 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 22, 2026 | DeltaNEC Interbody SystemK261279 · OVE | 510(k) clearances |
| Oct 14, 2025 | PressON Spinal Fixation SystemK253331 · NKB | 510(k) clearances |
| Apr 30, 2025 | Stable-L Lumbar Interbody SystemK243934 · OVD | 510(k) clearances |
| Jul 17, 2024 | Stable-C Interbody SystemK241467 · OVE | 510(k) clearances |
| Mar 20, 2024 | Tranquil-L Interbody SystemK233375 · MAX | 510(k) clearances |
| Mar 12, 2024 | Tranquil-C Interbody SystemK240416 · ODP | 510(k) clearances |
| Oct 26, 2023 | PressON Spinal Fixation SystemK233234 · NKB | 510(k) clearances |
| Oct 12, 2023 | Stable-L Standalone Lumbar Interbody SystemK231486 · OVD | 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
