FDA Device Establishments · JSON-LD · Markdown

ONDINE RESEARCH LABORATORIES/ONDINE BIOMEDICAL INC. (US)

FEI 3006845489 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active

FEI Number3006845489
Owner / OperatorOndine Biomedical Inc. (#10049666)
Address19017 120TH AVE NE STE 102, Bothell, WA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)EQH
Regulation § (21 CFR)874.4350
Proprietary namesPeriowave Light Diffusing Tip

External sources

Source: openFDA. Public-domain (CC0).