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Parker Quality & Compliance

PQC Reg Watch

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Device type

Densitometer, Bone

Product code KGI · Class II · 21 CFR 892.1170 · Radiology

FDA classification database

Recent 510(k)s

Sep 11, 2026

K254072

BoneVue

Curvebeam AI / Curvebeam, LLC

Recent recalls

No recalls in the archive for KGI.