510(k) Report

FDA applicant

Fitness Motivation Institute of America

Mchenry, IL1 decision1981–19810 recalls

FDA records 1 decision for Fitness Motivation Institute of America (Mchenry, IL) in 1981: 1 510(k) clearance. All are in product code KTZ (Caliper). 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 Fitness Motivation Institute of America’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fitness Motivation Institute of America since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Fitness Motivation Institute of America by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • KTZCaliper1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K810116Isorobic Skinfold CaliperFitness Motivation Institute of America · 19811cites it

What has FDA decided for it lately?

  • K810116Isorobic Skinfold CaliperFitness Motivation Institute of America · 1981

The one decision as Fitness Motivation Institute of America →

Other applicant names beginning “Fitness”

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

Fitness Quest, Inc. 2Fitness Equipment Co., Inc. 1Fitness TO Go, Inc. 1