510(k) Report

FDA applicant

Coritechs, Inc.

New Haven, CT1 decision1992–19920 recalls

FDA records 1 decision for Coritechs, Inc. (New Haven, CT) in 1992: 1 510(k) clearance. All are in product code HAW (Neurological Stereotaxic Instrument). 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 Coritechs, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Coritechs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • HAWNeurological Stereotaxic Instrument1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K915791Coritaxic Multi-Modal Stereotaxi WorkstationCoritechs, Inc. · 19921cites it

What has FDA decided for it lately?

  • K915791Coritaxic Multi-Modal Stereotaxi WorkstationCoritechs, Inc. · 1992

The one decision as Coritechs, Inc. →