FDA applicant

Kent Design & Manufacturing, Inc.

Grand Rapids, MI6 decisions1986–19860 recalls

FDA records 6 decisions for Kent Design & Manufacturing, Inc. (Grand Rapids, MI) in 1986: 6 510(k) clearances. All are in product code IKK (System, Isokinetic Testing And Evaluation). 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, physical medicine panel, where it files most

How often FDA has decided Kent Design & Manufacturing, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kent Design & Manufacturing, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kent Design & Manufacturing, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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See the 510(k) Report

Other applicant names beginning “Kent”

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

Kent Laboratories, Inc. 40 Kent Imaging, Inc. 5 Kent Barker & Assoc. 1 Kent J. Toone, D.D.S. 1 Kent Medical Devices, Inc. 1

Kent Design & Manufacturing, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Kent”