FDA Device Establishments · JSON-LD · Markdown

EIKON DEVICE INC.

FEI 3010363542 · Export Device to the United States But Perform No Other Operation on Device · Status: Active

FEI Number3010363542
Owner / OperatorEikon Device Inc. (#10044469)
Address689 Innovation Drive, Kingston Ontario, K7K 7E6, CA
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)FME
Regulation § (21 CFR)880.6265
Proprietary namesGraham drape sheet

External sources

Source: openFDA. Public-domain (CC0).