510(k) Report

FDA applicant

Advanced Vascular Dynamics

Portland, OR8 decisions2004–20150 recalls

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, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Advanced Vascular Dynamics’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2007: 12009: 22010: 12014: 22015: 1
2007high 2 (2009) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Advanced Vascular Dynamics by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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