510(k) Report

FDA applicant

Creation North America, Inc.

Milwaukee, WI1 decision1990–19900 recalls

FDA records 1 decision for Creation North America, Inc. (Milwaukee, WI) in 1990: 1 510(k) clearance. All are in product code EIH (Powder, Porcelain). 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 Creation North America, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Creation North America, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Creation North America, 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?

  • EIHPowder, Porcelain1decision

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.

  • K900209Willi Geller Ceramic Creation & SurpriseCreation North America, Inc. · 19901cites it

What has FDA decided for it lately?

  • K900209Willi Geller Ceramic Creation & SurpriseCreation North America, Inc. · 1990

The one decision as Creation North America, Inc. →