Kinova

FDA Filings

This page includes the latest FDA filings for Kinova. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3009538853
FEI Number3009538853
NameRon Borgschulte
Owner & OperatorKinova
Contact Address4333 Boulevard de la Grande-Allee
Boisbriand CA-QC Quebec J7H 1M7 CA
Official Correspondent
  • Annie Duchesne
  • 1-514-2773777-4185
US Agent
Importing Logistics Registration
ImporterPartners in Medicine
Address11469 Olive Blvd. Suite 127
Saint Louis, MO 63141 UNITED STATES
Importer TypeDistributor
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address11469 Olive Blvd
Creve Coeur, MO 63141 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Ron Borgschulte [Kinova]
Kinova Lift Arm2019-06-27
Ron Borgschulte [Kinova]
Kinova Dynamic arm support O540 V22018-03-30
Ron Borgschulte [Kinova]
MICO2013-09-19
Ron Borgschulte [Kinova]
JACO2013-09-19

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