FDA applicant

Schaerer Mayfield USA, Inc.

Cincinnati, OH2 decisions2005–20060 recalls

FDA records 2 decisions for Schaerer Mayfield USA, Inc. (Cincinnati, OH) from 2005 to 2006: 2 510(k) clearances. Most are in product codes HAW (Neurological Stereotaxic Instrument) and JAK (System, X-Ray, Tomography, Computed). Its devices cite 2 predicates, 0 of them its own earlier devices. 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Schaerer Mayfield USA, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Schaerer Mayfield USA, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?