FDA applicant

Baurs Krey Assoc., Inc.

Mchenry, IL4 decisions1984–19840 recalls

FDA records 4 decisions for Baurs Krey Assoc., Inc. (Mchenry, IL) in 1984: 4 510(k) clearances. Most are in product codes DWL (Stocking, Medical Support (To Prevent Pooling…) and GBI (Material, External Aesthetic Restoration, Used…). 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 hospital panel, where it files most

How often FDA has decided Baurs Krey Assoc., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Baurs Krey Assoc., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Baurs Krey Assoc., Inc.

Which product codes does it file in?

What has FDA decided for it lately?