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Kinesia 360

Great Lakes Neurotechnologies Inc. · Model 502-0265, Sensor Lower · UDI-DI 00859584006089

GYD Prescription
1
510(k) clearances
3
Adverse events
0
Recalls
5
Facilities

Description

Kinesia 360, Sensor Lower

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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.