FDA Device Establishments · JSON-LD · Markdown

RadiusXR Inc.

FEI 3014397047 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Repack or Relabel Medical Device Manufacture Medical Device · Status: Active

FEI Number3014397047
Owner / OperatorRadiusXR, Inc. (#10049603)
Address5994 W LAS POSITAS BLVD STE 101, Pleasanton, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)HPT
Regulation § (21 CFR)886.1605
Proprietary namesRadius Inspire

External sources

Source: openFDA. Public-domain (CC0).