FDA applicant

Ann Arbor Digital Devices

Ann Arbor, MI1 decision2005–20050 recalls

FDA records 1 decision for Ann Arbor Digital Devices (Ann Arbor, MI) in 2005: 1 510(k) clearance. All are in product code MQB (Solid State X-Ray Imager (Flat Panel/Digital…). 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 Ann Arbor Digital Devices’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ann Arbor Digital Devices since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ann Arbor Digital Devices

Which product codes does it file in?

What has FDA decided for it lately?