Device Recall iCup

Manufacturer

  • Manufacturer Address
    Ameditech Inc, 9940 Mesa Rim Rd, San Diego CA 92121-2910
  • Source
    USFDA

5 devices with a similar name

Learn more about the data here

  • Model / Serial
    143037 143106 144152 144218 152456 152457 152698 153048 153129 153201 153385 153648
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution.
  • Product Description
    iCup DX 10 Panel w/Adulterant, Item No. I-DXA-1107-142
  • Manufacturer
  • Model / Serial
    143345 143442 151537 152163 152334 152674 152697 153075 153127 153216 153390 153499 153634
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution.
  • Product Description
    iCup DX 12 Panel w/ Adulterant, Item No. I-DXA-1127-023
  • Manufacturer
  • Model / Serial
    141971 142195 142397 142674 142997 144209 144463 150018 150883 151525 151526 152180 152741 153045 153150 153151 153211 153376 153650
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution.
  • Product Description
    iCup DX 8 Panel w/Adulterant, Item No. I-DXA-187-016
  • Manufacturer