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 Spectrum Vascular with 6 510(k) clearances. The most recent is a 510(k) clearance dated Aug 10, 2026: Unimpregnated Central Venous 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.
| Aug 10, 2026 | Unimpregnated Central Venous CatheterK260165 · FOZ | 510(k) clearances |
| Jun 26, 2026 | Arterial Pressure Monitoring Set/TrayK261455 · DQO | 510(k) clearances |
| Mar 25, 2026 | Arterial Pressure Monitoring Set/TrayK254278 · DQO | 510(k) clearances |
| Dec 16, 2025 | BioFlo Hybrid PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology; BioFlo Midline Catheter; Xcela Power Injectable PICC; Xcela PICC with PASV Valve Technology; Xcela Hybrid PICC with PASV Valve TechnologyK252373 · LJS | 510(k) clearances |
| Jul 30, 2025 | Intraosseous Infusion NeedlesK250724 · FMI | 510(k) clearances |
| Nov 27, 2024 | SV Spectrum MRC Central Venous Catheter; SV Spectrum MR Central Venous Catheter; SV Central Venous CatheterK241115 · FOZ | 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
