510(k) Report

FDA applicant

Trent Wells, Inc.

Walker, MI1 decision1981–19810 recalls

FDA records 1 decision for Trent Wells, Inc. (Walker, MI) in 1981: 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 Trent Wells, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Trent Wells, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Trent Wells, 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 3 times; 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.

  • K811452Brown-Roberts-Wells Stereotaxic SytemTrent Wells, Inc. · 19813cite it

What has FDA decided for it lately?

  • K811452Brown-Roberts-Wells Stereotaxic SytemTrent Wells, Inc. · 1981

The one decision as Trent Wells, Inc. →