FDA applicant

Cameo, Inc.

Toledo, OH3 decisions1992–19930 recalls

FDA records 3 decisions for Cameo, Inc. (Toledo, OH) from 1992 to 1993: 3 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and HIO (Sampler, Amniotic Fluid (Amniocentesis Tray)). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Cameo, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cameo, Inc.

Which product codes does it file in?

What has FDA decided for it lately?