SnapshotGLO (KB100)— 510(k) K242669

Substantially Equivalent

Kent Imaging, Inc.

FDA 510(k) clearance K242669 for SnapshotGLO (KB100), Substantially Equivalent on 2025-03-26. Applicant: Kent Imaging, Inc.. Device class: 2.

Clearance details

Applicant: Kent Imaging, Inc.
Product code: Code QJF
Device class: Class 2
Regulation: 21 CFR 878.4550
Advisory panel: General, Plastic Surgery
Date received: 2024-09-05
Decision date: 2025-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Calgary, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code QJF

K251678 — Swift Ray 12026-02-24
K230734 — Multispectral Imager Kit (MSI Kit) (300-00015), Multispectral Imager (MSI) (300-00009)2023-12-05
K213840 — MolecuLight I:X2022-05-18
K211901 — MolecuLightDX2021-07-21
K210882 — MolecuLight I:X2021-06-22

More clearances from Kent Imaging, Inc.

K240601 — SnapshotNIR model KD2052024-04-02
K163070 — Kent Camera2017-05-05
K113507 — KENT CAMERA2012-08-08

Recalls naming K242669

K-number listed on FDA's recall record

Z-2775-2026 — SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.Class II·Ongoing·KENT IMAGING, INC.·20260630

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K242669.

Data sourced from openFDA. This site is unofficial and independent of the FDA.