FDA applicant

Izon Business Products, Inc.

West Nyack, NY4 decisions1995–20010 recalls

FDA records 4 decisions for Izon Business Products, Inc. (West Nyack, NY) from 1995 to 2001: 4 510(k) clearances. Most are in product codes JXA (Kit, Screening, Urine) and PJE (Blood/Plasma Collection Device For Dna Testing). 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, microbiology panel, where it files most

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

FDA decisions per year

No FDA decision for Izon Business Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Izon Business Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?