FDA applicant
Spectrum Vascular
FDA records 6 decisions for Spectrum Vascular (White Plains, NY) from 2024 to 2026: 6 510(k) clearances. Most are in product codes FOZ (Catheter, Intravascular, Therapeutic…) and DQO (Catheter, Intravascular, Diagnostic). Since 2016 its 510(k)s took a median of 141 days from receipt to decision, against 156 for FDA’s reviews in the same codes and years. Its devices cite 7 predicates, 1 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Spectrum Vascular’s devices, and how often a recall has named them.
FDA decisions per year
2in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2024.
Planning a device like Spectrum Vascular’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Spectrum”
FDA records each applicant name separately; these may or may not be the same firm.