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Fore Health

FORTECHGRP CO., LTD. · Model ACT8000-TX · UDI-DI 04719883871435

SDV
0
510(k) clearances
18
Adverse events
0
Recalls
107
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.