FDA applicant

Ladd Research Industries, Inc.

Burlington, VT3 decisions1986–19890 recalls

FDA records 3 decisions for Ladd Research Industries, Inc. (Burlington, VT) from 1986 to 1989: 3 510(k) clearances. All are in product code GWM (Device, Monitoring, Intracranial Pressure). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Ladd Research Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ladd Research Industries, Inc.

Which product codes does it file in?

What has FDA decided for it lately?