510(k) Report

FDA applicant

Vuetek Scientific, LLC

Marietta, GA1 decision2011–20110 recalls

FDA records 1 decision for Vuetek Scientific, LLC (Marietta, GA) in 2011: 1 510(k) clearance. All are in product code KZA (Device, Vein Location, Liquid Crystal). 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 hospital panel, where it files most

How often FDA has decided Vuetek Scientific, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2011: 1
2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Vuetek Scientific, LLC by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • KZADevice, Vein Location, Liquid Crystal1decision

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.

  • K101838VTS1000Vuetek Scientific, LLC · 20111cites it

What has FDA decided for it lately?

  • K101838VTS1000Vuetek Scientific, LLC · 2011

The one decision as Vuetek Scientific, LLC →