FDA applicant

Everapex Design & Marketing Corp.

Taipei, TW1 decision1996–19960 recalls

FDA records 1 decision for Everapex Design & Marketing Corp. (Taipei, TW) 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 Everapex Design & Marketing Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Everapex Design & Marketing Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Everapex Design & Marketing Corp.

Which product codes does it file in?

What has FDA decided for it lately?