FDA Device Establishments · JSON-LD · Markdown

EOSERA INC

FEI 3013559620 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device · Status: Active

FEI Number3013559620
Owner / OperatorEosera Inc (#10058317)
Address5000 South Freeway, Suite 106, Fort Worth, TX, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)OGQ
Regulation § (21 CFR)880.6960
Proprietary namesEar Irrigation Kit with irrigation bulb syringe; Wax Blaster MD Ear Irrigation and Cleaning Kit with Ear Clean MD

External sources

Source: openFDA. Public-domain (CC0).