510(k) Report

FDA applicant

Mtd, Inc.

Mchenry, IL5 decisions1977–20070 recalls

FDA records 5 decisions for Mtd, Inc. (Mchenry, IL) from 1977 to 2007: 5 510(k) clearances. Most are in product codes KPR (System, X-Ray, Stationary) and LLZ (System, Image Processing, Radiological). 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, radiology panel, where it files most

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

FDA decisions per year

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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