FDA applicant

Steven H. Warnock, M.D.

Sandy, UT1 decision2006–20060 recalls

FDA records 1 decision for Steven H. Warnock, M.D. (Sandy, UT) in 2006: 1 510(k) clearance. All are in product code FRP (Holder, Infant Position). 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 Steven H. Warnock, M.D.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Steven H. Warnock, M.D. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Steven”

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

Steven Frank Mercereau 1 Steven B. Lamberg, Dds 1 Steven K. Juhn 1 Steven K. Sue 1 Steven Chen 1 Steven Lamberg, D.D.S 1

Steven H. Warnock, M.D.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Steven”