Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IrelandLabelled 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 Perfuze with 12 510(k) clearances. The most recent is a 510(k) clearance dated Aug 12, 2026: Millipede 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.
| Date | Record | Source |
|---|---|---|
| Aug 12, 2026 | Millipede SystemK262399 · NRY | 510(k) clearances |
| Jul 9, 2026 | Millipede88 Access CatheterK253901 · QJP | 510(k) clearances |
| Mar 16, 2026 | Millipede SystemK253590 · NRY | 510(k) clearances |
| Aug 29, 2025 | Millipede70 Aspiration Catheter; Perfuze Aspiration Tube SetK252392 · NRY | 510(k) clearances |
| Feb 26, 2025 | Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube SetK250012 · NRY | 510(k) clearances |
| Oct 17, 2024 | Zipline Access CatheterK240711 · QJP | 510(k) clearances |
| Sep 20, 2024 | Millipede 088 Access Catheter; Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube SetK242504 · NRY | 510(k) clearances |
| Dec 14, 2023 | Millipede 088 Access CatheterK233648 · QJP | 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
