FDA Device Establishments · JSON-LD · Markdown

EMBOLX INC.

FEI 3011660785 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active

FEI Number3011660785
Owner / OperatorEmbolx Inc. (#10049613)
Address530 Lakeside Dr Ste 150, Sunnyvale, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)MJN
Regulation § (21 CFR)870.4450
Proprietary namesEmbolx Microcatheter

External sources

Source: openFDA. Public-domain (CC0).