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KForce Muscle Controller

Model K Push V3 · KINVENT BIOMECANIQUE · DI 03770011995370

LBB — Dynamometer, Ac-Powered · Class II · 21 CFR 888.1240

UDILibrary device dossier · generated 2026-09-12 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.

Recall history (0)

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Adverse-event reports — MAUDE (0)

Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.

No dated reports to chart.

Regulatory clearances

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Manufacturer compliance record — KINVENT BIOMECANIQUE

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