Facility

KINOVA

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

Key facts

1recalls · worst Class I

—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)	3009538853
Establishment type	Manufacture Medical Device
Location	4333 Grande-Allee Boisbriand Quebec, CA J7H 1M7
Registration status	Active · expires 2026
Parent company	Kinova (owner-operator 10045047)
Brand names	Kinova Dynamic arm support O540; Kinova Dynamic arm support O110

Activity by year

Recalls (1)

Devices registered here (1)

Orthosis, Limb Brace
Product code IQI (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.3475

Recalls & enforcement

Class IOngoing2024-08-22
Potential installation issue that could result in a fire hazard in the event of an interaction between a damaged Jaco arm and a wheelchair exhibiting electrical leakage.

All facilities operated by Kinova

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. “KINOVA (FEI 3009538853) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3009538853-kinova/

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