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ACCLARENT AERA

ACCLARENT, INC. · Model EU061655Z · UDI-DI 20705031230870

PNZ Prescription
1
510(k) clearances
31
Adverse events
0
Recalls
16
Facilities

Description

ACCLARENT AERA EUSTACHIAN TUBE BALLOON DILATION SYSTEM, 1 PK

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.