FDA applicant

Viox Corp.

Seattle, WA2 decisions1987–19870 recalls

FDA records 2 decisions for Viox Corp. (Seattle, WA) in 1987: 2 510(k) clearances. All are in product code IWR (Holder, Syringe, Lead). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Viox Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Viox Corp.

Which product codes does it file in?

What has FDA decided for it lately?