FDA applicant

East Health Development Group, Inc.

Tustin, CA1 decision1996–19960 recalls

FDA records 1 decision for East Health Development Group, Inc. (Tustin, CA) in 1996: 1 510(k) clearance. All are in product code IRO (Vibrator, Therapeutic). 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, physical medicine panel, where it files most

How often FDA has decided East Health Development Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for East Health Development Group, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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East Health Development Group, Inc.

Which product codes does it file in?

What has FDA decided for it lately?