Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009538853

FEI Number

3009538853

Entity Name

KINOVA

City/State/Country

Boisbriand Quebec, CA

Establishment Address

4333 Grande-Allee, Boisbriand Quebec J7H 1M7, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Kinova (Owner Number: 10045047)

Owner / Operator Contact Address

4333 Boulevard de la Grande-Allee, Boisbriand, CA-QC J7H 1M7, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

JACO Kinova Lift Arm Kinova Dynamic arm support O540 Kinova Dynamic arm support O110

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IQZ	Hand, External Limb Component, Powered	Physical Medicine	Class 1	890.3420	2013-09-19
KNO	Accessories, Wheelchair	Physical Medicine	Class 1	890.3910	2019-06-27
IQI	Orthosis, Limb Brace	Physical Medicine	Class 1	890.3475	2018-03-30

Official Correspondent

Keven Frechette

US Agent Details

Ron Borgschulte Business: Partners in Medicine LLC Email: ron@partnersinmed.com Phone: (314) 3242470

Related Public Records

Same Entity

Kinova

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009538853. Last updated year: 2026. Please use registration number 3009538853 when referencing this establishment in official correspondence.