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Eargo 6

Eargo, Inc. · Model 99-0147-001 · UDI-DI 00850010429366

QUH
1
510(k) clearances
14
Adverse events
0
Recalls
30
Facilities

Description

Eargo 6 System

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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.