FDA applicant
Advanced Vascular Dynamics
FDA records 8 decisions for Advanced Vascular Dynamics (Portland, OR) from 2004 to 2015: 8 510(k) clearances. Most are in product codes DXC (Clamp, Vascular) and JOM (Plethysmograph, Photoelectric, Pneumatic Or…). Its devices cite 12 predicates, 3 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 Advanced Vascular Dynamics’s devices, and how often a recall has named them.
FDA decisions per year
1in 2015
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Advanced Vascular Dynamics’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) Report