510(k) Report

FDA applicant

Med ET AL Development

Matthews, NC1 decision1995–19950 recalls

FDA records 1 decision for Med ET AL Development (Matthews, NC) in 1995: 1 510(k) clearance. All are in product code LQX (Device, Finger-Sucking). 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, physical medicine panel, where it files most

How often FDA has decided Med ET AL Development’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Med ET AL Development since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Med ET AL Development 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?

  • LQXDevice, Finger-Sucking1decision

What has FDA decided for it lately?

  • K945537T-GuardMed ET AL Development · 1995

The one decision as Med ET AL Development →