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Well-Life

WELL-LIFE HEALTHCARE LTD. · Model WL-2306E · UDI-DI 04719872263029

NUH NYN

510(k) clearances

118

Adverse events

Recalls

169

Facilities

Description

Well-Life Mini TENS Stimulator (WL-23XXC/WL-23XXE Series) Intended for temporary relief of pain Same associated with sore and aching muscles in the upper and lower extremities (arm and/or leg) due to strain from exercise or normal household and work activities.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.