FDA Device Establishments · JSON-LD · Markdown

SONENDO, INC.

FEI 3010817521 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active

FEI Number3010817521
Owner / OperatorSonendo, Inc. (#10046931)
Address26061 Merit Circle, Suite 101, Laguna Hills, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)EIF
Regulation § (21 CFR)872.4565
Proprietary namesErgo Arm

External sources

Source: openFDA. Public-domain (CC0).