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MotionSense Digital Goniometer

ENMOVI LTD · Model 007-00066-US · UDI-DI 15060808320092

KQX Prescription
10
510(k) clearances
0
Adverse events
0
Recalls
44
Facilities

Description

MotionSense Digital Goniometer

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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.