FDA Device Establishments · JSON-LD · Markdown

FIRST USE LLC

FEI 3005370013 · Repack or Relabel Medical Device · Status: Active

FEI Number3005370013
Owner / OperatorFIRST USE LLC (#9077490)
Address2500 SANDERSVILLE RD., LEXINGTON, KY, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)HRH
Regulation § (21 CFR)886.4350
Proprietary namesGAYHEART CORNEAL TREPHINE

External sources

Source: openFDA. Public-domain (CC0).