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Digital Knee®

OPUM TECHNOLOGIES SERVICES LIMITED · Model DK-013 · UDI-DI 09413000113839

KQX Prescription
10
510(k) clearances
0
Adverse events
0
Recalls
45
Facilities

Description

Digital Knee sensor is attached to a brace or orthosis and worn by a patient to collect motion data and assist with management of their condition.

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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.