FDA Device Establishments · JSON-LD · Markdown

TRANSLITE

FEI 3000205606 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active

FEI Number3000205606
Owner / OperatorTransLite,LLC (#9023110)
Address345 Commerce Green Blvd, SUGAR LAND, TX, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)IBJ
Regulation § (21 CFR)864.3600
Proprietary namesVEINLITE220; VEINLITE II; VEINLITE; NEVOSCOPE

External sources

Source: openFDA. Public-domain (CC0).