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COFOE

Cofoe Medical Technology Co.,Ltd · Model ICS920-B · UDI-DI 06950715500095

QUF

510(k) clearances

Adverse events (1 deaths)

Recalls

Facilities

Description

In-ear hearing aid, single ear (ABS, battery replacement, hearing aid size: 16*12*20 (mm)

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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.