FDA applicant

Vermont Diamond Instruments

Bridgewater Corners, VT2 decisions1991–19920 recalls

FDA records 2 decisions for Vermont Diamond Instruments (Bridgewater Corners, VT) from 1991 to 1992: 2 510(k) clearances. Most are in product codes EHJ (Disk, Abrasive) and EJL (Bur, Dental). 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 Vermont Diamond Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vermont Diamond Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Vermont”

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

Vermont Medical, Inc. 9 Vermont Wood Industries, Inc. 1

Vermont Diamond Instruments

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Vermont”