FDA applicant

Arno Intl., Inc.

Plantation, FL2 decisions1993–19930 recalls

FDA records 2 decisions for Arno Intl., Inc. (Plantation, FL) in 1993: 2 510(k) clearances. Most are in product codes HPC (Set, Lens, Trial, Ophthalmic) and HQZ (Frame, Spectacle). 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 Arno Intl., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Arno Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Arno Intl., Inc.

Which product codes does it file in?

What has FDA decided for it lately?