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DARCO® Relief Dual®

Darco (Europe) GmbH · Model RD-M1 · UDI-DI 00609271242012

KNP

510(k) clearances

120

Adverse events

Recalls

207

Facilities

Description

MS Grey Square-toe

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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.