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KENT IMAGING, INC.

2 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA. recall (Z-2775-2026)KENT IMAGING, INC.2026-07-22
Snapshot NIR, REF: KD204 recall (Z-0789-2024)KENT IMAGING, INC.2024-01-25

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