FDA applicant

Calliope Corp.

Mchenry, IL3 decisions1983–19840 recalls

FDA records 3 decisions for Calliope Corp. (Mchenry, IL) from 1983 to 1984: 3 510(k) clearances. Most are in product codes HQC (Unit, Phacofragmentation) and HQE (Instrument, Vitreous Aspiration And Cutting…). 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 Calliope Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Calliope Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Calliope Corp.

Which product codes does it file in?

What has FDA decided for it lately?