Facility

ImmersiveTouch, Inc.

1 recall(s) on record — most severe on record: Class III.

Key facts

1recalls · worst Class III

2inspections · worst VAI

—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)	3014833795
Establishment type	Manufacture Medical Device
Location	910 West Van Buren Street Chicago, IL, US 60607
Registration status	Active · expires 2026
Parent company	ImmersiveTouch (owner-operator 10058372)
Brand names	ImmersiveView Surgical Plan

Activity by year

Recalls (1)
Inspections (2)

Devices registered here (2)

Driver, Wire, And Bone Drill, Manual
Product code DZJ (opens in a new tab) · Class II · Dental · 21 CFR 872.4120
System, Image Processing, Radiological
Product code LLZ (opens in a new tab) · Class II · Radiology · 21 CFR 892.2050

Recalls & enforcement

Class IIIOngoing2020-04-03
Observed an internal repetitive software glitch in ImmersiveView.

FDA inspections (2)

NAI2023-09-14
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
NAI2020-01-29
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

All facilities operated by ImmersiveTouch

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. “ImmersiveTouch, Inc. (FEI 3014833795) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3014833795-immersivetouch-inc/

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