FDA applicant

Siemens Burdick, Inc.

Miltoon, WI7 decisions1991–19920 recalls

FDA records 7 decisions for Siemens Burdick, Inc. (Miltoon, WI) from 1991 to 1992: 7 510(k) clearances. Most are in product codes LOS (Unnamed device) and IOL (Treadmill, Powered). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Siemens Burdick, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Siemens Burdick, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?