Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Kent Imaging with 5 510(k) clearances and 2 device recalls. The most recent is a device recall dated Jun 30, 2026: SnapshotGLO Wound Imaging Device, Model KB100, KB100AA..
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Jun 30, 2026 | SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.Class II · The software controlling the wound imaging device's battery charging circuit was not designed to recognize and recover a | Device recalls |
| Mar 26, 2025 | SnapshotGLO (KB100)K242669 · QJF | 510(k) clearances |
| Apr 2, 2024 | SnapshotNIR model KD205K240601 · MUD | 510(k) clearances |
| Oct 30, 2023 | Snapshot NIR, REF: KD204Class II · Tissue oxygenation measurement system touchscreens may be unresponsive, which may prevent the viewing of oxygenation ima | Device recalls |
| Nov 10, 2020 | SnapshotNIRK201976 · MUD | 510(k) clearances |
| May 5, 2017 | Kent CameraK163070 · MUD | 510(k) clearances |
| Aug 8, 2012 | KENT CAMERAK113507 · MUD | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
