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Hetaida

Hetaida Technology Co., Ltd · Model K5102US · UDI-DI 06970289035649

INB
0
510(k) clearances
239
Adverse events (5 deaths)
0
Recalls
113
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.