FDA Device Establishments · JSON-LD · Markdown

KEGO CORPORATION

FEI 3008603863 · Export Device to the United States But Perform No Other Operation on Device · Status: Active

FEI Number3008603863
Owner / OperatorKEGO Corporation (#10052258)
Address4350 Castleton Rd., Unit 3-4, London Ontario, N6N 0A3, CA
Mandatory US AgentFDAbasics
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)ILT
Regulation § (21 CFR)890.5050
Proprietary namesADAPTOR, RECREATIONAL, MULTIPLE TYPES

External sources

Source: openFDA. Public-domain (CC0).