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 Walk Vascular with 9 510(k) clearances. The most recent is a 510(k) clearance dated Feb 1, 2022: JETi AIO Peripheral 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.
| Feb 1, 2022 | JETi AIO Peripheral Thrombectomy SystemK213565 · QEZ | 510(k) clearances |
| Nov 17, 2020 | JETi AIO Peripheral Thrombectomy SystemK201998 · QEZ | 510(k) clearances |
| Dec 9, 2019 | JETi Peripheral Thrombectomy SystemK192439 · QEZ | 510(k) clearances |
| Apr 17, 2019 | JETi 88 Peripheral Thrombectomy SystemK183403 · QEZ | 510(k) clearances |
| Oct 24, 2017 | ClearLumen II Peripheral Thrombectomy SystemK172000 · QEZ | 510(k) clearances |
| Feb 21, 2017 | ClearLumen II Peripheral Thrombectomy SystemK163051 · QEZ | 510(k) clearances |
| Oct 18, 2016 | ClearLumen II Thrombectomy SystemK161786 · QEZ | 510(k) clearances |
| Dec 2, 2014 | CLEARLUMEN THROMBECTOMY SYSTEMK140296 · QEZ | 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
