FDA applicant

Mpl Technologies, Inc.

Franklin Park, IL1 decision1997–19970 recalls

FDA records 1 decision for Mpl Technologies, Inc. (Franklin Park, IL) in 1997: 1 510(k) clearance. All are in product code KIF (Resin, Root Canal Filling). 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 Mpl Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mpl Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mpl Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?