FDA applicant

Cascades Device Consulting Associates

Bend, OR1 decision2010–20100 recalls

FDA records 1 decision for Cascades Device Consulting Associates (Bend, OR) in 2010: 1 510(k) clearance. All are in product code ELW (Material, Impression). 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, dental panel, where it files most

How often FDA has decided Cascades Device Consulting Associates’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Cascades Device Consulting Associates by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Cascades Device Consulting Associates’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

Other applicant names beginning “Cascades”

FDA records each applicant name separately; these may or may not be the same firm.

Cascades Psh, Inc. 1

Cascades Device Consulting Associates

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cascades”