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 its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Vy Spine with 21 510(k) clearances. The most recent is a 510(k) clearance dated Mar 27, 2026: VyPlate™ Anterior Cervical Plate 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.
| Mar 27, 2026 | VyPlate™ Anterior Cervical Plate SystemK260697 · KWQ | 510(k) clearances |
| Mar 19, 2026 | DiversiVy™ Facet Screw SystemK253432 · MRW | 510(k) clearances |
| Jan 7, 2026 | VyBrate™ VBR SystemK253158 · MQP | 510(k) clearances |
| Mar 18, 2025 | FortiVy™ OsteoVy™ Lumbar IBFK241783 · MAX | 510(k) clearances |
| Oct 16, 2024 | Vy Spine™ VyLam™ Laminoplasty SystemK242784 · NQW | 510(k) clearances |
| Sep 24, 2024 | LumiVy™ Lumbar IBF SystemK233807 · MAX | 510(k) clearances |
| Oct 30, 2023 | ClariVy™ Cervical IBF SystemK231836 · ODP | 510(k) clearances |
| Oct 13, 2023 | VyLink™ Spinal Screw SystemK231744 · NKB | 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
