510(k) Report

FDA applicant

Neomatrix, LLC

Irvine, CA1 decision2002–20020 recalls

FDA records 1 decision for Neomatrix, LLC (Irvine, CA) in 2002: 1 510(k) clearance. All are in product code KNW (Instrument, Biopsy). Its devices cite 3 predicates, 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Neomatrix, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Neomatrix, LLC’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?

  • KNWInstrument, Biopsy1decision

Whose devices does it build on?

Its devices cite 3 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K020848NAFD 100Neomatrix, LLC · 2002

The one decision as Neomatrix, LLC →