FDA Device Establishments · JSON-LD · Markdown

KINETIQSENSE

FEI 3047516614 · Manufacture Medical Device · Status: Active

FEI Number3047516614
Owner / OperatorKinetIQSense (#10095958)
Address700 W Research Center Blvd Ste 1409, Fayetteville, AR, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)PJO
Regulation § (21 CFR)880.2400
Proprietary namesKiQMove

External sources

Source: openFDA. Public-domain (CC0).