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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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Biomaterials
KEYSTONE DENTAL, INC.
10.210.1060
In Commercial Distribution

  • D7681021010600 ()

  • .5cc - 5cc
10.210.1060

  • Dental bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.210.1050
In Commercial Distribution

  • D7681021010500 ()

  • .5cc - 5cc
10.210.1050

  • Dental bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.120.1070
In Commercial Distribution

  • D7681012010700 ()

  • .5cc - 5cc
10.120.1070

  • Dental bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.120.1060
In Commercial Distribution

  • D7681012010600 ()

  • .5cc - 5cc
10.120.1060

  • Dental bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.120.1050
In Commercial Distribution

  • D7681012010500 ()

  • .5cc - 5cc
10.120.1050

  • Dental bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.110.1070
In Commercial Distribution

  • D7681011010700 ()

  • .5cc - 5cc
10.110.1070

  • Dental bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.110.1060
In Commercial Distribution

  • D7681011010600 ()

  • .5cc - 5cc
10.110.1060

  • Dental bone matrix implant, human-derived
Biomaterials
KEYSTONE DENTAL, INC.
10.110.1050
In Commercial Distribution

  • D7681011010500 ()

  • .5cc - 5cc
10.110.1050

  • Dental bone matrix implant, human-derived
No Description
Hans Biomed Corp.
FG100
In Commercial Distribution

  • 08809204339945 ()


  • Bone matrix implant, human-derived
No Description
Hans Biomed Corp.
FG050
In Commercial Distribution

  • 08809204339938 ()


  • Bone matrix implant, human-derived
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