Facility

VIRTUAL INCISION CORPORATION

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

Key facts

1recalls · 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)	3030285773
Establishment type	Manufacture Medical Device
Location	1501 Old Cheney Rd Lincoln, NE, US 68512
Registration status	Active · expires 2026
Parent company	Virtual Incision Corporation (owner-operator 10090552)
Brand names	MIRA Surgical System

Activity by year

Recalls (1)

Devices registered here (1)

Table Mounted Miniaturized Electromechanical Surgical System
Product code SAB (opens in a new tab) · Class II · General, Plastic Surgery · 21 CFR 878.4962

Recalls & enforcement

Class IICompleted2025-04-23
The MIRA Surgical System Software Version 4.0.3 loaded on the Surgeon Control Console may have the potential to exhibit interrupted motion on the display screen, caused by a software latency between the movement of the hand controllers and the movement of the Surgical Minibot arm…

All facilities operated by Virtual Incision Corporation

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. “VIRTUAL INCISION CORPORATION (FEI 3030285773) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3030285773-virtual-incision-corporation/

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