FDA applicant

Bruker Medical Imaging, Inc.

Lisle, IL7 decisions1989–19920 recalls

FDA records 7 decisions for Bruker Medical Imaging, Inc. (Lisle, IL) from 1989 to 1992: 7 510(k) clearances. All are in product code LNH (System, Nuclear Magnetic Resonance Imaging). 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 Bruker Medical Imaging, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bruker Medical Imaging, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Bruker”

FDA records each applicant name separately; these may or may not be the same firm.

Bruker Daltonik GmbH 3 Bruker Daltonics, Inc. 3

Bruker Medical Imaging, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Bruker”