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Soundbright

Xiamen Vienatone Medical Technology Co., Ltd. · Model Mini · UDI-DI 06973967150177

QUF
0
510(k) clearances
39
Adverse events (1 deaths)
0
Recalls
81
Facilities

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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.