FDA applicant

Sorex Medical

Salt Lake City, UT9 decisions1989–19940 recalls

FDA records 9 decisions for Sorex Medical (Salt Lake City, UT) from 1989 to 1994: 9 510(k) clearances. Most are in product codes LDQ (Unnamed device) and FYD (Apparatus, Exhaust, Surgical). 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 hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Sorex Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Sorex Medical

Which product codes does it file in?

What has FDA decided for it lately?