KENT IMAGING, INC.
KENT IMAGING, INC. appears in FDA public data with 2 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2775-2026, Class II) was initiated on June 30, 2026. Its most recent 510(k) clearance was granted on March 26, 2025.
Summary
- Total Recalls
- 2
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-2775-2026 | Class II | SnapshotGLO Wound Imaging Device, Model KB100, KB100AA. | June 30, 2026 |
| Z-0789-2024 | Class II | Snapshot NIR, REF: KD204 | October 30, 2023 |