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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.
10.120.1070
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
BIOMET MICROFIXATION, INC
02-3110
In Commercial Distribution

  • 00888233025195 ()
02-3110

  • Bone matrix implant, human-derived
No Description
BIOMET MICROFIXATION, INC
02-3105
In Commercial Distribution

  • 00888233025188 ()
02-3105

  • Bone matrix implant, human-derived
No Description
BIOMET MICROFIXATION, INC
02-3102
In Commercial Distribution

  • 00888233025171 ()
02-3102

  • Bone matrix implant, human-derived
No Description
BIOMET MICROFIXATION, INC
02-3101
In Commercial Distribution

  • 00888233025164 ()
02-3101

  • Bone matrix implant, human-derived
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