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

Show Filters

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
AlloFuse® DBM Putty, 1 cc
ALLOSOURCE
90038001
In Commercial Distribution

  • M536900380011 ()

  • 1 cc
90038001

  • Bone matrix implant, human-derived
i-FACTOR™ Putty, 5.0 cc Syringe
Cerapedics Inc.
700-050
In Commercial Distribution

  • M8517000501 ()
700-050

  • Bone matrix implant, animal-derived, bioabsorbable
Maxima Gutta Percha CC 20/Vl
HENRY SCHEIN, INC.
1018674
In Commercial Distribution

  • H65810186749 ()
  • H65810186741 ()
1018674

  • Synthetic gutta-percha
Maxima Gutta Percha CC 20/Vl
HENRY SCHEIN, INC.
1018528
In Commercial Distribution

  • H65810185289 ()
  • H65810185281 ()
1018528

  • Synthetic gutta-percha
Maxima Gutta Percha CC 20/Vl
HENRY SCHEIN, INC.
1018247
In Commercial Distribution

  • H65810182479 ()
  • H65810182471 ()
1018247

  • Synthetic gutta-percha
Maxima Gutta Percha CC 20/Vl
HENRY SCHEIN, INC.
1017594
In Commercial Distribution

  • H65810175949 ()
  • H65810175941 ()
1017594

  • Synthetic gutta-percha
< 1 ... 53 54 55 56 57 ... 122 >