510(k) Report

FDA applicant

Neogen Technologies, Inc.

Ft Lauderdale, FL1 decision2003–20030 recalls

FDA records 1 decision for Neogen Technologies, Inc. (Ft Lauderdale, FL) in 2003: 1 510(k) clearance. All are in product code OMP (Negative Pressure Wound Therapy Powered…). 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 Neogen Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Neogen Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Neogen Technologies, Inc. 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?

  • OMPNegative Pressure Wound Therapy Powered Suction Pump1decision

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.

  • K032301Neogen One, Closed Wound Drain System, Part Number: NG9900Neogen Technologies, Inc. · 20031cites it

What has FDA decided for it lately?

  • K032301Neogen One, Closed Wound Drain System, Part Number: NG9900Neogen Technologies, Inc. · 2003

The one decision as Neogen Technologies, Inc. →