510(k) Report

FDA applicant

The Jayms Co.

Lindon, UT1 decision1996–19960 recalls

FDA records 1 decision for The Jayms Co. (Lindon, UT) in 1996: 1 510(k) clearance. All are in product code HCC (Device, Biofeedback). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 The Jayms Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Jayms Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like The Jayms Co.’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

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K924313Digital Conductance MeterThe Jayms Co. · 1996

The one decision as The Jayms Co. →