FDA applicant

Magnatone Hearing Aid Corp.

Casselberry, FL8 decisions1985–19970 recalls

FDA records 8 decisions for Magnatone Hearing Aid Corp. (Casselberry, FL) from 1985 to 1997: 8 510(k) clearances. All are in product code ESD (Hearing Aid, Air-Conduction, Prescription). 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, ear, nose and throat panel, where it files most

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

FDA decisions per year

No FDA decision for Magnatone Hearing Aid Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Magnatone”

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

Magnatone Hearing Aid Corp. Dba Persona Medical 1

Magnatone Hearing Aid Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Magnatone”