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ALLESEE AOA-PRO · Model 3000-0032 · UDI-DI 00889989038583

KMY Prescription
10
510(k) clearances
1,679
Adverse events
0
Recalls
112
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.