510(k) Report

FDA applicant

Lifestyle Hearing, Inc.

Tucson, AR1 decision1993–19930 recalls

FDA records 1 decision for Lifestyle Hearing, Inc. (Tucson, AR) in 1993: 1 510(k) clearance. 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 Lifestyle Hearing, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lifestyle Hearing, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • ESDHearing Aid, Air-Conduction, Prescription1decision

What has FDA decided for it lately?

  • K932189IN-the-Ear Hearing AidLifestyle Hearing, Inc. · 1993

The one decision as Lifestyle Hearing, Inc. →

Other applicant names beginning “Lifestyle”

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

The Lifestyle Co., Inc. 3Lifestyle Safety Products (Hui Zhou) Co., Ltd. 1Lifestyle Safty Products (Hui Zhou) Co., Ltd. 1