510(k) Report

FDA applicant

Med-General Technologies, LLC

Naples, FL1 decision2004–20040 recalls

FDA records 1 decision for Med-General Technologies, LLC (Naples, FL) in 2004: 1 510(k) clearance. All are in product code FSY (Light, Surgical, Ceiling Mounted). 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, general and plastic surgery panel, where it files most

How often FDA has decided Med-General Technologies, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Med-General Technologies, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Med-General Technologies, LLC 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?

  • FSYLight, Surgical, Ceiling Mounted1decision

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.

  • K042382Dual Led Lite Engine with Illumination Led Cable Coupled to a Led Lite HeadMed-General Technologies, LLC · 20041cites it

What has FDA decided for it lately?

  • K042382Dual Led Lite Engine with Illumination Led Cable Coupled to a Led Lite HeadMed-General Technologies, LLC · 2004

The one decision as Med-General Technologies, LLC →