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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 Gel, 1cc
ALLOSOURCE
ABS-2002-01
In Commercial Distribution

  • M536ABS2002011 ()

  • 1 cc
ABS-2002-01

  • Bone matrix implant, human-derived
STIMUBLAST® DBM Putty, 5cc
ALLOSOURCE
ABS-2001-05
In Commercial Distribution

  • M536ABS2001051 ()

  • 5 cc
ABS-2001-05

  • Bone matrix implant, human-derived
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
Optium DBM Putty
LIFENET HEALTH
TPUT10
In Commercial Distribution

  • 00889858517744 ()

  • 10 cc
TPUT10

  • Bone matrix implant, human-derived
Optium DBM Putty
LIFENET HEALTH
TPUT05
In Commercial Distribution

  • 00889858517720 ()

  • 5 cc
TPUT05

  • Bone matrix implant, human-derived
Optium DBM Putty
LIFENET HEALTH
TPUT02
In Commercial Distribution

  • 00889858517706 ()

  • 2.5 cc
TPUT02

  • Bone matrix implant, human-derived
Optium DBM Putty
LIFENET HEALTH
TPUT01
In Commercial Distribution

  • 00889858517683 ()

  • 1 cc
TPUT01

  • Bone matrix implant, human-derived
Optium DBM Gel
LIFENET HEALTH
TGEL10
In Commercial Distribution

  • 00889858450584 ()

  • 10 cc
TGEL10

  • Bone matrix implant, human-derived
Optium DBM Gel
LIFENET HEALTH
TGEL05
In Commercial Distribution

  • 00889858450560 ()

  • 5 cc
TGEL05

  • Bone matrix implant, human-derived
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