FDA Device Establishments · JSON-LD · Markdown

BENIK CORP.

FEI 3023878 · Manufacture Medical Device · Status: Active

FEI Number3023878
Owner / OperatorBENIK CORP. (#3023860)
Address11871 SILVERDALE WAY N.W., No. 107, Silverdale, WA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)ITQ
Regulation § (21 CFR)890.3475
Proprietary namesBENIK

External sources

Source: openFDA. Public-domain (CC0).