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MILLENNIUM

Avalign Technologies, Inc. · Model 2-4246 · UDI-DI 00190776323356

KAS Prescription
1
510(k) clearances
7
Adverse events (1 deaths)
0
Recalls
80
Facilities

Description

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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.