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Widex

Widex A/S · Model D-FS · UDI-DI 05706069722017

OSM

510(k) clearances

673

Adverse events

Recalls

Facilities

Description

Widex D-FS BTE (Midnight black S-220 ) Telecoil, RC coil

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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.