FDA Device Establishments · JSON-LD · Markdown

KISO EHF

FEI 3038620647 · Manufacture Medical Device · Status: Active

FEI Number3038620647
Owner / OperatorKiso ehf (#10093544)
AddressHatun 12, Reykjavik, 105, IS
Mandatory US AgentKiso INC
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)HCC
Regulation § (21 CFR)882.5050
Proprietary namesKineMotion

External sources

Source: openFDA. Public-domain (CC0).