FDA applicant

Micro-Ear Technology, Inc.

Plymouth, MN5 decisions1993–20040 recalls

FDA records 5 decisions for Micro-Ear Technology, Inc. (Plymouth, MN) from 1993 to 2004: 5 510(k) clearances. Most are in product codes ESD (Hearing Aid, Air-Conduction, Prescription) and KLW (Masker, Tinnitus). 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 Micro-Ear Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Micro-Ear Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Micro-Ear Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?