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 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Sequent Medical with 4 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Feb 18, 2017: VIA 17 Microcatheter.
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 18, 2017 | VIA 17 MicrocatheterK162565 · DQY | 510(k) clearances |
| Sep 23, 2016 | VIA 27 Microcatheter, Part No. FG27-154-01, Model No. VIA-27-154-01 The VIA 27 is intended for the introduction of non-liquid interventiClass II · Sequent Medical is recalling the VIA 27 Microcatheter because it may not adequately re-sheath the interventional device | Device recalls |
| Aug 28, 2015 | VIA 21 MicrocatheterK150894 · DQY | 510(k) clearances |
| Dec 20, 2013 | VIA MICROCATHETER, VIA PLUS MICROCATHETERK132652 · DQY | 510(k) clearances |
| Mar 19, 2013 | VIA MICROCATHETER, VIA PLUS MICROCATHETERK123477 · KRA | 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
