510(k) Report

FDA applicant

Unitech

Madison, WI1 decision1995–19950 recalls

FDA records 1 decision for Unitech (Madison, WI) in 1995: 1 510(k) clearance. All are in product code HCC (Device, Biofeedback). 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 Unitech’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Unitech since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Unitech’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • HCCDevice, Biofeedback1decision

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.

  • K935853Emg TrainerUnitech · 19951cites it

What has FDA decided for it lately?

The one decision as Unitech →