510(k) Report

FDA applicant

Well-Life Consultant

Taipei, TW1 decision2001–20010 recalls

FDA records 1 decision for Well-Life Consultant (Taipei, TW) in 2001: 1 510(k) clearance. All are in product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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, neurology panel, where it files most

How often FDA has decided Well-Life Consultant’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Well-Life Consultant since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Well-Life Consultant 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?

  • GZJStimulator, Nerve, Transcutaneous, For Pain Relief1decision

Who builds on its devices?

Later devices cite its devices 4 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K002874Well-TensWell-Life Consultant · 20014cite it

What has FDA decided for it lately?

  • K002874Well-TensWell-Life Consultant · 2001

The one decision as Well-Life Consultant →

Other applicant names beginning “Well-Life”

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

Well-Life Healthcare Limited 29Well Lead Medical Co., Ltd. 17Well Lead Medical Instruments 4Well Brain International, Ltd. 4Well Success Biotech, Inc. 3Well Lead Medical (Hainan) Co., Ltd. 1Well Arts Optical Factory, Ltd. 1Well Lead Instruments 1Well Care (Wuhan) Medical Technology Co., Ltd. 1Well Being Ent. 1Well Home Health Products Co. 1