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FDA PRODUCT CODE · CLASS II

SAORadiology Software For Opportunistic Evaluation Of Low Bone Mineral Density

This device is software which opportunistically assesses radiological images to estimate bone mineral density (BMD) intended to assist in a healthcare professional's decision to evaluate patients for possible low BMD within a bone health screening program. The software employs an algorithm that estimates BMD using eligible radiological image data obtained for other clinical purposes.

DEVICE CLASS
Class II
REGULATION
21 CFR 892.1171
MEDICAL SPECIALTY
Radiology
REVIEW PANEL
RA
ImplantLife-sustainingGMP-exemptThird-party review eligible
2
510(K)/PMA CLEARANCES
510k: 2
0
RECALL ENTRIES

Recent clearances

K253192Alpha Intelligence Manifolds, Inc. · 510k2026-06-10
K251408Naitive Technologies, Ltd. · 510k2025-09-02

Related on SPEQ

Medical devices industryMedical device quality (ISO 13485)FDA device clearancesFDA enforcement & recalls

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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