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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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STIMUBLAST® DBM Putty, 1cc
ALLOSOURCE
ABS-2001-01
In Commercial Distribution

  • M536ABS2001011 ()

  • 1 cc
ABS-2001-01

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

  • M536901380101 ()

  • 10 cc
90138010

  • Bone matrix implant, human-derived
Bioactive Bone Graft Matrix, 14 cc Moldable Puck
Spine Wave, Inc.
11-5804
In Commercial Distribution

  • 10840642159653 ()

  • 14 cc


  • Bone matrix implant, animal-derived, bioabsorbable
Bioactive Bone Graft Matrix, 7 cc Moldable Puck
Spine Wave, Inc.
11-5803
In Commercial Distribution

  • 10840642159646 ()

  • 7 cc


  • Bone matrix implant, animal-derived, bioabsorbable
Bioactive Bone Graft Matrix, 40 cc Moldable Strip
Spine Wave, Inc.
11-5802
In Commercial Distribution

  • 10840642159639 ()

  • 40 cc


  • Bone matrix implant, animal-derived, bioabsorbable
Bioactive Bone Graft Matrix, 10 cc Moldable Strip
Spine Wave, Inc.
11-5800
In Commercial Distribution

  • 10840642159615 ()

  • 10 cc


  • Bone matrix implant, animal-derived, bioabsorbable
Bioactive Bone Graft Matrix, 20 cc Moldable Strip
Spine Wave, Inc.
11-5801
In Commercial Distribution

  • 10840642159622 ()

  • 20 cc


  • Bone matrix implant, animal-derived, bioabsorbable
NATRELLE 133SX With Sut Tab, 800cc
Allergan, Inc.
133SX-16-T
Not in Commercial Distribution

  • 10888628004634 ()

  • 800 cc
133SX-16-T

  • Skin-port tissue expander
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