510(k) Report

FDA applicant

Medical Advances, Inc.

Milwaukee, WI57 decisions1989–20020 recalls

FDA records 57 decisions for Medical Advances, Inc. (Milwaukee, WI) from 1989 to 2002: 57 510(k) clearances. Most are in product codes LNH (System, Nuclear Magnetic Resonance Imaging) and MOS (Coil, Magnetic Resonance, Specialty). 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 Medical Advances, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Advances, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medical Advances, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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