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 Inquis Medical with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jul 27, 2026: Powered Aventus Thrombectomy 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 27, 2026 | Powered Aventus Thrombectomy System™K261105 · QEZ | 510(k) clearances |
| Jul 15, 2026 | Aventus Thrombectomy SystemK262030 · QEZ | 510(k) clearances |
| Apr 13, 2026 | Aventus Introducer SheathK260091 · DYB | 510(k) clearances |
| Jan 15, 2026 | Aventus Thrombectomy SystemK253925 · QEZ | 510(k) clearances |
| Jun 13, 2025 | Aventus Thrombectomy SystemK251189 · QEW | 510(k) clearances |
| Mar 25, 2025 | Aventus Thrombectomy System (IM-2100)K250668 · QEW | 510(k) clearances |
| Feb 26, 2025 | Aventus Thrombectomy SystemK250202 · QEW | 510(k) clearances |
| May 14, 2024 | Aventus Clot Management SystemK240426 · CAC | 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
