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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LOGIC Distractor, Right 36mm
OSTEOMED LLC
216-0113
In Commercial Distribution

  • 00845694004336 ()

  • Distraction Curve Radius = 36mm
216-0113

  • Implantable craniofacial bone distractor
LOGIC Distractor, Left 36mm
OSTEOMED LLC
216-0112
In Commercial Distribution

  • 00845694004329 ()

  • Distraction Curve Radius = 36mm
216-0112

  • Implantable craniofacial bone distractor
LOGIC Distractor, Right 52mm
OSTEOMED LLC
216-0111
In Commercial Distribution

  • 00845694004312 ()

  • Distraction Curve Radius = 52mm
216-0111

  • Implantable craniofacial bone distractor
LOGIC Distractor, Left 52mm
OSTEOMED LLC
216-0110
In Commercial Distribution

  • 00845694004305 ()

  • Distraction Curve Radius = 52mm
216-0110

  • Implantable craniofacial bone distractor
Activation Wire Removal Tool
OSTEOMED LLC
216-0103
In Commercial Distribution

  • 00845694004299 ()
216-0103

  • General internal orthopaedic fixation system implantation kit
Distraction Tool
OSTEOMED LLC
216-0102
In Commercial Distribution

  • 00845694004282 ()
216-0102

  • General internal orthopaedic fixation system implantation kit
Logic Distraction Organizer Block
OSTEOMED LLC
216-0000
In Commercial Distribution

  • 00845694004275 ()
216-0000

  • General internal orthopaedic fixation system implantation kit
Logic Jr Distractor, 30mm Right
OSTEOMED LLC
216-1006
In Commercial Distribution

  • 00842528123188 ()

  • length of distraction
  • Length: 30 Millimeter
216-1006

  • Implantable craniofacial bone distractor
Logic Jr Distractor, 30mm Left
OSTEOMED LLC
216-1005
In Commercial Distribution

  • 00842528123171 ()

  • length of distraction
  • Length: 30 Millimeter
216-1005

  • Implantable craniofacial bone distractor
220-0121, Purple ID Tag, 2.0/2.4 DL
OSTEOMED LLC
220-0643-63
In Commercial Distribution

  • 00845694061636 ()
220-0643-63

  • General internal orthopaedic fixation system implantation kit
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