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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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ALIF TRIAL 12° 28 X 38 X 18
Corentec Co., Ltd
SI.C20.0418
In Commercial Distribution

  • 08800017285276 ()


  • Spinal implant trial
ALIF TRIAL 12° 28 X 38 X 17
Corentec Co., Ltd
SI.C20.0417
In Commercial Distribution

  • 08800017285269 ()


  • Spinal implant trial
LOSPA IS DLIF Cage (Non-sterile)
Corentec Co., Ltd
SC.V08.6016
In Commercial Distribution

  • 08800017222936 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS DLIF Cage (Non-sterile)
Corentec Co., Ltd
SC.V08.6014
In Commercial Distribution

  • 08800017222929 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS DLIF Cage (Non-sterile)
Corentec Co., Ltd
SC.V08.6012
In Commercial Distribution

  • 08800017222912 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS DLIF Cage (Non-sterile)
Corentec Co., Ltd
SC.V08.5516
In Commercial Distribution

  • 08800017222905 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS DLIF Cage (Non-sterile)
Corentec Co., Ltd
SC.V08.5514
In Commercial Distribution

  • 08800017222899 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS DLIF Cage (Non-sterile)
Corentec Co., Ltd
SC.V08.5512
In Commercial Distribution

  • 08800017222882 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS DLIF Cage (Non-sterile)
Corentec Co., Ltd
SC.V08.5016
In Commercial Distribution

  • 08800017222875 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS DLIF Cage (Non-sterile)
Corentec Co., Ltd
SC.V08.5014
In Commercial Distribution

  • 08800017222868 ()


  • Polymeric spinal interbody fusion cage
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