FDA applicant

Kenneth Ullrich

Wenatchee, WA1 decision1995–19950 recalls

FDA records 1 decision for Kenneth Ullrich (Wenatchee, WA) in 1995: 1 510(k) clearance. All are in product code EWO (Audiometer). 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 Kenneth Ullrich’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kenneth Ullrich since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Kenneth”

FDA records each applicant name separately; these may or may not be the same firm.

Kenneth Hilsen 1 Kenneth J. Hoek, M.D., Inc. 1 Kenneth J. Purcell 1 Kenneth Chapman 1

Kenneth Ullrich

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Kenneth”