Facility

Kent Imaging Inc

2 recall(s) on record — most severe on record: Class II.

Key facts

2recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3009771004
Establishment type	Manufacture Medical Device
Location	Suite 300, 1210 8th Street SW Calgary Alberta, CA T2R 1L3
Registration status	Active · expires 2026
Parent company	Kent Imaging Inc. (owner-operator 10041732)
Brand names	SnapshotNIR

Activity by year

Recalls (2)

Devices registered here (1)

Oximeter, Tissue Saturation
Product code MUD (opens in a new tab) · Class II · Cardiovascular · 21 CFR 870.2700

Recalls & enforcement

Class IIOngoing2026-06-30
The software controlling the wound imaging device's battery charging circuit was not designed to recognize and recover a battery that has fully discharged into a low-power "shipping mode." When this occurs, an affected device will not resume charging when reconnected to power and…
Class IIOngoing2023-10-30
Tissue oxygenation measurement system touchscreens may be unresponsive, which may prevent the viewing of oxygenation images.

All facilities operated by Kent Imaging Inc.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Kent Imaging Inc (FEI 3009771004) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3009771004-kent-imaging-inc/

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