FDA Device Establishments · JSON-LD · Markdown

UNITED STATES ENDOSCOPY GROUP, INC.

FEI 1000122656 · Repack or Relabel Medical Device · Status: Active

FEI Number1000122656
Owner / OperatorSTERIS Corporation (#10078069)
Address5976 Heisley Rd, Mentor, OH, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)PTM
Regulation § (21 CFR)870.1650
Proprietary namesLUMIFLEX Balloon Inflator

External sources

Source: openFDA. Public-domain (CC0).