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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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AlloFuse® Plus DBM Putty, 5cc
ALLOSOURCE
90338005
In Commercial Distribution

  • M536903380051 ()

  • 5 cc
90338005

  • Bone matrix implant, human-derived
AlloFuse® Plus DBM Paste, 8cc
ALLOSOURCE
90238008
In Commercial Distribution

  • M536902380081 ()

  • 8 cc
90238008

  • Bone matrix implant, human-derived
AlloFuse® Plus DBM Paste, 3 cc
ALLOSOURCE
90238003
In Commercial Distribution

  • M536902380031 ()

  • 3 cc
90238003

  • Bone matrix implant, human-derived
AlloFuse® Plus DBM Paste, 1 cc
ALLOSOURCE
90238001
In Commercial Distribution

  • M536902380011 ()

  • 1 cc
90238001

  • Bone matrix implant, human-derived
AlloFuse® DBM Gel, 10cc
ALLOSOURCE
90138010
In Commercial Distribution

  • M536901380101 ()

  • 10 cc
90138010

  • Bone matrix implant, human-derived
AlloFuse® DBM Gel, 5 cc
ALLOSOURCE
90138005
In Commercial Distribution

  • M536901380051 ()

  • 5 cc
90138005

  • Bone matrix implant, human-derived
AlloFuse® DBM Gel, 1 cc
ALLOSOURCE
90138001
In Commercial Distribution

  • M536901380011 ()

  • 1 cc
90138001

  • Bone matrix implant, human-derived
AlloFuse® DBM Putty, 10 cc
ALLOSOURCE
90038010
In Commercial Distribution

  • M536900380101 ()

  • 10 cc
90038010

  • Bone matrix implant, human-derived
AlloFuse® DBM Putty, 5 cc
ALLOSOURCE
90038005
In Commercial Distribution

  • M536900380051 ()

  • 5 cc
90038005

  • Bone matrix implant, human-derived
AlloFuse® DBM Putty, 2.5 cc
ALLOSOURCE
90038002
In Commercial Distribution

  • M536900380021 ()

  • 2.5 cc
90038002

  • Bone matrix implant, human-derived
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