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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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X OSTEOTOME 7MM X 17 IN
Smith & Nephew, Inc.
71369207
In Commercial Distribution

  • 03596010407207 ()
71369207

  • Orthopaedic osteotome
Case 6.5 x 18 x 1.5
INNOMED, INC.
9008
In Commercial Distribution

  • 00840277131744 ()
9008

  • Device sterilization/disinfection container, reusable
RASP 14 X 10 X 9
MEDTRONIC SOFAMOR DANEK, INC.
EX0718044
In Commercial Distribution

  • 00763000180843 ()


  • Bone file/rasp, manual, reusable
RASP 14 X 10 X 6
MEDTRONIC SOFAMOR DANEK, INC.
EX0718041
In Commercial Distribution

  • 00763000180812 ()


  • Bone file/rasp, manual, reusable
RASP 14 X 10 X 5
MEDTRONIC SOFAMOR DANEK, INC.
EX0718040
In Commercial Distribution

  • 00763000180805 ()


  • Bone file/rasp, manual, reusable
RASP 14 X 10 X 8
MEDTRONIC SOFAMOR DANEK, INC.
EX0718043
In Commercial Distribution

  • 00763000180836 ()


  • Bone file/rasp, manual, reusable
TRIAL L12 x W14 x H10
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298999 ()
AC.2022

  • Bone-screw internal spinal fixation system, non-sterile
TRIAL L12 x W14 x H9
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298982 ()
AC.2021

  • Bone-screw internal spinal fixation system, non-sterile
TRIAL L12 x W14 x H8
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298975 ()
AC.2020

  • Bone-screw internal spinal fixation system, non-sterile
TRIAL L12 x W14 x H7
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809489298968 ()
AC.2019

  • Bone-screw internal spinal fixation system, non-sterile
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