FDA applicant

Fonar Corp.

Melville, NY12 decisions1988–20060 recalls

FDA records 12 decisions for Fonar Corp. (Melville, NY) from 1988 to 2006: 12 510(k) clearances. All are in product code LNH (System, Nuclear Magnetic Resonance Imaging). Its devices cite 3 predicates, 2 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, radiology panel, where it files most

How often FDA has decided Fonar Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fonar Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Fonar Corp.

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?