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Kinova

Canada·CA-MF-000003231

Last updated September 17, 2026

Information

Country
Canada
Address
4333, boul. Grande-Allée, Boisbriand, Canada
Website
kinova.ca
LinkedIn
—
Facebook
—
Phone
5142773777
PRRC Contact
Genevieve St-Jean
EUDAMED SRN
CA-MF-000003231
FDA FEI Number
3009538853
DUNS Number
—

Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
OLED Display PD 0508 0001-01
EUDAMED
Class IActive
Jaco Blue Universal Interface KR UI3 0001
EUDAMED
Class IActive
Universal Interface V2 PC 0000 0003-01
EUDAMED
Class IActive
Lift Arm KR8600-01
EUDAMED
Class IActive
Jaco® AO 0000 0001
EUDAMED
Class IActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Aug 22, 2024Z-0049-2025—open, classified

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.