510(k) Report

FDA applicant

Zila, Inc.

Phoenix, AZ1 decision2008–20080 recalls

FDA records 1 decision for Zila, Inc. (Phoenix, AZ) in 2008: 1 510(k) clearance. All are in product code NXV (Diagnostic Light, Soft Tissue Detector). 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, dental panel, where it files most

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

FDA decisions per year

1in 2008

2008: 1
2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Zila, Inc. by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • NXVDiagnostic Light, Soft Tissue Detector1decision

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.

  • K080043Vizilite EyewearZila, Inc. · 20081cites it

What has FDA decided for it lately?

  • K080043Vizilite EyewearZila, Inc. · 2008

The one decision as Zila, Inc. →