# KINETIQSENSE

FEI: 3047516614
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: KinetIQSense (#10095958)

Address: 700 W Research Center Blvd Ste 1409, Fayetteville, AR, US



## Products

Total registered: 1
Top product codes: PJO
Regulation §: 880.2400

Proprietary names: KiQMove

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223047516614%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3047516614