FDA applicant

Cranco Co.

Salt Lake City, UT1 decision1987–19870 recalls

FDA records 1 decision for Cranco Co. (Salt Lake City, UT) in 1987: 1 510(k) clearance. All are in product code CAO (Airway, Esophageal (Obturator)). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Cranco Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cranco Co.

Which product codes does it file in?

What has FDA decided for it lately?