Kent Imaging, Inc.
Kent Imaging, Inc. holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2025, with 2 FDA device recalls on record.
Top product codes for Kent Imaging, Inc.
FDA recalls by Kent Imaging, Inc.
- Z-2775-2026 — SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
- Z-0789-2024 — Snapshot NIR, REF: KD204
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Kent Imaging, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.