Manufacturer registered with FDA

ImmersiveTouch

Chicago, IL, United States. Lists 1 dental device type with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator10058372Manufacturer

Device types listed: 1
Brands and models: 1
510(k) clearances: 12020–2020
Markets registered in: 1United States
Establishments: 1United States

510(k) clearances per year, 2007–2026

Devices listed with FDA

What ImmersiveTouch currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Manual Wire Driver and Bone DrillDZJ · Class 2	Surgical drills & motors	Maker	ImmersiveView Surgical Plan	2020

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

510(k) clearances

Clearances on which FDA names ImmersiveTouch as the applicant.

Decided	510(k)	Device	Device type
9 Jun 2020	K181813	ImmersiveView Surgical Plan (IVSP®)	DZJ Manual Wire Driver and Bone Drill

Registered establishments

Establishment	Location	What it does
ImmersiveTouch, Inc.FDA reg. 3014833795	Chicago, IL, United States	Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10058372). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.