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Anterior Mouthpiece

ZYRIS, INC. · Model CAM0201 · UDI-DI 00810032660352

DYNEIF
10
510(k) clearances
100
Adverse events (1 deaths)
0
Recalls
151
Facilities

Description

Anterior Mouthpiece, 10-Pack, Medium

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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.