FDA applicant

Holgrath Medical Technologies, Inc.

Cheshire, CT6 decisions1995–19960 recalls

FDA records 6 decisions for Holgrath Medical Technologies, Inc. (Cheshire, CT) from 1995 to 1996: 6 510(k) clearances. Most are in product codes BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)) and 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 Holgrath Medical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Holgrath Medical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Holgrath Medical Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?