FDA applicant

Peter Stevens, MD

Salt Lake City, UT1 decision2005–20050 recalls

FDA records 1 decision for Peter Stevens, MD (Salt Lake City, UT) in 2005: 1 510(k) clearance. All are in product code KTT (Appliance, Fixation, Nail/Blade/Plate…). 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, orthopedic panel, where it files most

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

FDA decisions per year

No FDA decision for Peter Stevens, MD since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Peter”

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

Peter Lazic GmbH 2 Peter Martin Associates, Inc. 1 Peter G. Finamore, Sr. 1 Peter Fischer 1 Peter M. Rothenberg, M.D. 1 Peter F. Lee, Inc. 1 Peter M. Tolliver 1

Peter Stevens, MD

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Peter”