FDA Device Establishments · JSON-LD · Markdown

RUNLITE S.A.

FEI 6347 · Manufacture Medical Device · Status: Active

FEI Number6347
Owner / OperatorRUNLITE SA (#8020160)
Address9 AVENUE DE LA COOPERATION, MICHEROUX, SOUMAGNE Liege, 4630, BE
Mandatory US AgentKinetec USA, Inc.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)FYH
Regulation § (21 CFR)878.3910
Proprietary namesX-Lite; 3D-Lite

External sources

Source: openFDA. Public-domain (CC0).