510(k) Report

FDA applicant

Ingredion Incorporated

Bridgewater1 decision1973–19730 recalls

FDA records 1 decision for Ingredion Incorporated (Bridgewater) in 1973: 1 original PMA approval. All are in product code KGP (Unnamed device). 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, general and plastic surgery panel, where it files most

How often FDA has decided Ingredion Incorporated’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ingredion Incorporated since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ingredion Incorporated 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?

  • KGPUnnamed device1decision

What has FDA decided for it lately?

  • N80535Absorbo (R) Dusting PowderIngredion Incorporated · 1973

The one decision as Ingredion Incorporated →