FDA Device Establishments · JSON-LD · Markdown

ULTRASPECT USA, LLC

FEI 3018788582 · Manufacture Medical Device · Status: Active

FEI Number3018788582
Owner / OperatorUltraSPECT USA, LLC (#10081545)
Address101 Dillion Court, Gray, TN, US
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)LLZ, KPS
Regulation § (21 CFR)892.2050, 892.1200
Proprietary namesXpress3.Cardiac including ASCS; Xpress.Cardiac including ACSC

External sources

Source: openFDA. Public-domain (CC0).