FDA Device Establishments · JSON-LD · Markdown

NEUROLIEF Ltd.

FEI 3015088397 · Export Device to the United States But Perform No Other Operation on Device Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active

FEI Number3015088397
Owner / OperatorNeurolief (#10081665)
Address12 Giborei Israel, Netanya Central, 4250412, IL
Mandatory US AgentNeurolief Inc.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)PCC
Regulation § (21 CFR)882.5891
Proprietary namesRelivion

External sources

Source: openFDA. Public-domain (CC0).