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Mothermed

Famidoc Technology Co.,Ltd. · Model ES408 · UDI-DI 00818218024080

NGX NUH GXY

510(k) clearances

Adverse events

Recalls

207

Facilities

Description

To be used for temporary relief of pain associated with sore and aching muscles due to strain from exercise or normal household work activities.

Recalls

Date	Firm	Reason
2021-01-13	BEMER INT. AG	There potential that electromagnetic fields generated in the therapy system may cause technical defects in a patient using an insulin pumps or a malfunction of a pacemaker.
2013-05-23	Pinook-Usa	Failure to submit a premarket submission and gain approval of a medical device.
2013-05-23	Pinook-Usa	Failure to submit a premarket submission and gain approval of a medical device.

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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.