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., part of StrykerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Inari Medical with 58 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Sep 18, 2026: Triever Duo Catheter.
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.
| Sep 18, 2026 | Triever Duo CatheterK253419 · QEW | 510(k) clearances |
| Aug 21, 2026 | Artix™ MT;Artix™ Thin-Walled SheathK262538 · QEW | 510(k) clearances |
| Dec 17, 2025 | Intri26 Introducer SheathK252508 · DYB | 510(k) clearances |
| Oct 29, 2025 | Protrieve SheathK253323 · QEW | 510(k) clearances |
| May 12, 2025 | InThrill™ Thrombectomy SystemK250421 · QEW | 510(k) clearances |
| Mar 13, 2025 | FlowTriever2 CatheterK250088 · QEW | 510(k) clearances |
| Oct 15, 2024 | Artix™ MT; Artix™ Thin-Walled Thrombectomy SheathK241894 · QEW | 510(k) clearances |
| Sep 27, 2024 | ClotTriever XL Catheter (41-102)K242557 · QEW | 510(k) clearances |
| Mar 23, 2020 | Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/ Aspiration System, UDI: 00850291007079Class II · The hemostasis valve of aspiration guide catheter devices may fail to seal resulting in a loss of vacuum during thrombus | Device recalls |
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
