510(k) Report

FDA applicant

Dynamic Functional Positioner, Inc.

Mchenry, IL1 decision1982–19820 recalls

FDA records 1 decision for Dynamic Functional Positioner, Inc. (Mchenry, IL) in 1982: 1 510(k) clearance. All are in product code KMY (Positioner, Tooth, Preformed). 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, dental panel, where it files most

How often FDA has decided Dynamic Functional Positioner, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dynamic Functional Positioner, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dynamic Functional Positioner, Inc. 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?

  • KMYPositioner, Tooth, Preformed1decision

What has FDA decided for it lately?

  • K821458Dynamic Funtional PositionerDynamic Functional Positioner, Inc. · 1982

The one decision as Dynamic Functional Positioner, Inc. →

Other applicant names beginning “Dynamic”

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

Dynamic Technology Corp. 4Dynamic Imaging, Inc. 3Dynamic Systems, Inc. 2Dynamic Marketing Ent. 1Dynamic Air, Inc. 1Dynamic Digital Displays, Inc. 1Dynamic Innovations, Inc. 1Dynamic Plantations Sdn Bhd 1Dynamic Healthcare Technologies, Inc. 1