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 13, 2026, FDA's public records list MiRus, LLC with 24 510(k) clearances. The most recent is a 510(k) clearance dated Mar 18, 2026: EUROPA™ Posterior Cervical Fusion Navigated Instruments.
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.
| Date | Record | Source |
|---|---|---|
| Mar 18, 2026 | EUROPA™ Posterior Cervical Fusion Navigated InstrumentsK253444 · OLO | 510(k) clearances |
| Feb 19, 2026 | ATLAS™ Expandable Osteotomy Wedge SystemK252733 · PLF | 510(k) clearances |
| Nov 19, 2024 | EUROPA™ Posterior Cervical Fusion SystemK242516 · NKG | 510(k) clearances |
| May 17, 2024 | MiRus MoRe Lumbar Plating SystemK241175 · KWQ | 510(k) clearances |
| Oct 27, 2023 | RIGEL™ 3DR Standalone Anterior Cervical Interbody Fusion SystemK232348 · OVE | 510(k) clearances |
| Oct 13, 2023 | RIGEL™ 3DR Anterior Cervical Corpectomy SystemK232481 · PLR | 510(k) clearances |
| Sep 11, 2023 | MiRus 3DR Lateral Lumbar Interbody Fusion System with Integrated Plate FixationK232154 · OVD | 510(k) clearances |
| Jun 23, 2023 | EUROPA™ Navigated InstrumentsK230369 · OLO | 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
