FDA applicant

Stortz

Saint Louis, MO1 decision1991–19910 recalls

FDA records 1 decision for Stortz (Saint Louis, MO) in 1991: 1 510(k) clearance. All are in product code ETF (Unit, Examining/Treatment, Ent). 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, ear, nose and throat panel, where it files most

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

FDA decisions per year

No FDA decision for Stortz since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Stortz

Which product codes does it file in?

What has FDA decided for it lately?