Facility

Intellijoint Surgical 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)	3010822102
Establishment type	Export Device to the United States But Perform No Other Operation on Device
Location	809 Wellington St. N Kitchener Ontario, CA N2H 5L6
Registration status	Active · expires 2026
Parent company	Intellijoint Surgical Inc. (owner-operator 10047431)
Brand names	Camera Drape

Activity by year

Recalls (2)

Devices registered here (1)

Drape, Surgical, Exempt
Product code PUI (opens in a new tab) · Class II · General, Plastic Surgery · 21 CFR 878.4370

Recalls & enforcement

Class IITerminated2020-02-11
During total knee arthroplasty (TKA), the software may incorrectly calculate femur resection depth.
Class IITerminated2019-06-28
Apple has determined that, in a limited number of older generation 15-inch MacBook Pro Units, the battery may overheat and pose a fire safety risk. To date, Intellijoint has distributed, 15-inch MacBook Pros which are the Workstation component (affected P/N 000-0241) in the Inte…

All facilities operated by Intellijoint Surgical 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. “Intellijoint Surgical Inc. (FEI 3010822102) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3010822102-intellijoint-surgical-inc/

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