FDA applicant

Angiolaz, Inc.

Bellows Falls, VT10 decisions1990–20000 recalls

FDA records 10 decisions for Angiolaz, Inc. (Bellows Falls, VT) from 1990 to 2000: 10 510(k) clearances. Most are in product codes FWF (Camera, Television, Endoscopic, Without Audio) and LYK (Angioscope). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Angiolaz, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Angiolaz, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Angiolaz, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?