FDA Device Establishments · JSON-LD · Markdown

Lazurite Inc.

FEI 3021744308 · Manufacture Medical Device · Status: Active

FEI Number3021744308
Owner / OperatorLazurite Inc. (#10061641)
Address4760 Richmond Road Suite 400, Cleveland, OH, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)GCJ
Regulation § (21 CFR)876.1500
Proprietary namesArthroFree

External sources

Source: openFDA. Public-domain (CC0).