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 its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Cagent Vascular, LLC with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 4, 2022: Serranator PTA Serration Balloon 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.
| Date | Record | Source |
|---|---|---|
| May 4, 2022 | Serranator PTA Serration Balloon CatheterK220704 · PNO | 510(k) clearances |
| Dec 15, 2021 | Serranator PTA Serration Balloon CatheterK213728 · PNO | 510(k) clearances |
| Dec 22, 2020 | Serranator PTA Serration Balloon CatheterK203437 · PNO | 510(k) clearances |
| Apr 15, 2020 | Serranator PTA Serration Balloon CatheterK193181 · PNO | 510(k) clearances |
| Feb 13, 2017 | Serranator Alto PTA Serration Balloon CatheterK163380 · PNO | 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
