FDA applicant

Neurodelivery Technology, Inc.

Lebanon, NH3 decisions1993–19940 recalls

FDA records 3 decisions for Neurodelivery Technology, Inc. (Lebanon, NH) from 1993 to 1994: 3 510(k) clearances. All are in product code CAZ (Anesthesia Conduction Kit). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Neurodelivery Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Neurodelivery Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?