FDA applicant

Vxtra Corp.

Mchenry, IL10 decisions1980–19830 recalls

FDA records 10 decisions for Vxtra Corp. (Mchenry, IL) from 1980 to 1983: 10 510(k) clearances. Most are in product codes HQC (Unit, Phacofragmentation) and GES (Blade, Scalpel). 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Vxtra Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Vxtra Corp.

Which product codes does it file in?

What has FDA decided for it lately?