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Kinesis QTUG

KINESIS · Model 3.2.2 · UDI-DI 05391542950003

PJP
0
510(k) clearances
33
Adverse events
0
Recalls
6
Facilities

Description

QTUG consists of a device for assessment of mobility, falls risk and frailty in older adults through quantitative analysis of movement using body-worn inertial sensors. The device streams data over a Bluetooth interface to an Android tablet device.

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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.