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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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BiomaX Bone Graft Putty Plus Chips, 10cc
Surgalign Spine Technologies, Inc.
BMX-0110
In Commercial Distribution

  • 00810076560694 ()

  • 10 cc


  • Bone matrix implant, human-derived
BiomaX Bone Graft Putty Plus Chips, 5cc
Surgalign Spine Technologies, Inc.
BMX-0105
In Commercial Distribution

  • 00810076560687 ()

  • 5 cc


  • Bone matrix implant, human-derived
BiomaX Bone Graft Putty Plus Chips, 2.5cc
Surgalign Spine Technologies, Inc.
BMX-0102
In Commercial Distribution

  • 00810076560670 ()

  • 2.5 cc


  • Bone matrix implant, human-derived
BiomaX Bone Graft Putty Plus Chips, 1cc
Surgalign Spine Technologies, Inc.
BMX-0101
In Commercial Distribution

  • 00810076560663 ()

  • 1 cc


  • Bone matrix implant, human-derived
BiomaX Bone Graft Putty, 10cc
Surgalign Spine Technologies, Inc.
BMX-0010
In Commercial Distribution

  • 00810076560656 ()

  • 10 cc


  • Bone matrix implant, human-derived
BiomaX Bone Graft Putty, 5cc
Surgalign Spine Technologies, Inc.
BMX-0005
In Commercial Distribution

  • 00810076560649 ()

  • 5 cc


  • Bone matrix implant, human-derived
BiomaX Bone Graft Putty, 2.5cc
Surgalign Spine Technologies, Inc.
BMX-0002
In Commercial Distribution

  • 00810076560380 ()

  • 2.5 cc


  • Bone matrix implant, human-derived
BiomaX Bone Graft Putty, 1cc
Surgalign Spine Technologies, Inc.
BMX-0001
In Commercial Distribution

  • 00810076560007 ()

  • 1 cc


  • Bone matrix implant, human-derived
INTEGRA Flowable Wound Matrix
Integra Lifesciences Corporation
FWD301
In Commercial Distribution

  • M269FWD3011 ()
  • 10381780032472 ()

  • 3 cc
FWD301

  • Wound protein matrix solution
DBM 005110 PRGENIX DBM 10 CC SRVC FEE
MEDTRONIC SOFAMOR DANEK, INC.
005110
Not in Commercial Distribution

  • 00613994247612 ()

  • 10 cc volume


  • Bone matrix implant, human-derived
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