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Oticon

Oticon A/S · Model 133879 · UDI-DI 05707131264985

OSM Prescription
1
510(k) clearances
700
Adverse events
0
Recalls
81
Facilities

Description

RIA, KIT 13 WL DIR 90 R H BE

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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.