FDA Device Establishments · JSON-LD · Markdown

Hiossen, Inc.

FEI 3031162123 · Manufacture Medical Device · Status: Active

FEI Number3031162123
Owner / OperatorHiossen Inc. (#10026425)
Address6940 Beach Blvd, Building D Unit D-709, Buena Park, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)NHA
Regulation § (21 CFR)872.3630
Proprietary namesET SMARTFit Abutment

External sources

Source: openFDA. Public-domain (CC0).