510(k) Report

FDA applicant

Hoggan Health Industries, Inc.

Draper, UT1 decision1986–19860 recalls

FDA records 1 decision for Hoggan Health Industries, Inc. (Draper, UT) in 1986: 1 510(k) clearance. All are in product code LBB (Dynamometer, Ac-Powered). 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 Hoggan Health Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hoggan Health Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Hoggan”

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