FDA applicant

Vermont Medical, Inc.

Bellows Falls, VT9 decisions1978–20030 recalls

FDA records 9 decisions for Vermont Medical, Inc. (Bellows Falls, VT) from 1978 to 2003: 9 510(k) clearances. Most are in product codes DRX (Electrode, Electrocardiograph) and GXY (Electrode, Cutaneous). 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 Vermont Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vermont Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Vermont Medical, Inc.’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 “Vermont”

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

Vermont Diamond Instruments 2 Vermont Wood Industries, Inc. 1

Vermont Medical, 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?

Other applicant names beginning “Vermont”