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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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BDS PROBE CC 3-6-8-11 MM #6 HANDLE
NORDENT MANUFACTURING INC
PCN8-11/6BH
In Commercial Distribution

  • 00840018603936 ()


  • Periodontal probe, reusable
ENDO INST GLICK #1, DL CC HAND
NORDENT MANUFACTURING INC
CEENG1-RL
In Commercial Distribution

  • 00840018633216 ()


  • Endodontic plugger
ENDO INST GLICK #1, DL CC HAND
NORDENT MANUFACTURING INC
CEENG1
In Commercial Distribution

  • 00840018633209 ()


  • Endodontic plugger
ENDO INST GLICK #1, DL CC HAND
NORDENT MANUFACTURING INC
CEENG1-RL
In Commercial Distribution

  • 00840018632929 ()


  • Manual endodontic filling material spreader
ENDO INST GLICK #1, DL CC HAND
NORDENT MANUFACTURING INC
CEENG1
In Commercial Distribution

  • 00840018632912 ()


  • Manual endodontic filling material spreader
COMPOSITE INST 6A TIN DL CC HA
NORDENT MANUFACTURING INC
CEPFI6AT
In Commercial Distribution

  • 00840018638105 ()


  • Margin finishing dental file/rasp, reusable
EXPRO DE PROBE N15 CC PROBE N22
NORDENT MANUFACTURING INC
CEPCN15-N22
In Commercial Distribution

  • 00840018647022 ()


  • Periodontal probe, reusable
AlloFuse® Plus DBM Putty, 10 cc
ALLOSOURCE
90338010
In Commercial Distribution

  • M536903380101 ()

  • 10 cc
90338010

  • Bone matrix implant, human-derived
AlloFuse® Plus DBM Paste, 3 cc
ALLOSOURCE
90238003
In Commercial Distribution

  • M536902380031 ()

  • 3 cc
90238003

  • Bone matrix implant, human-derived
AlloFuse® Plus DBM Paste, 1 cc
ALLOSOURCE
90238001
In Commercial Distribution

  • M536902380011 ()

  • 1 cc
90238001

  • Bone matrix implant, human-derived
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