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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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Duplex Abutment Φ3.5/GH3.5/PH7.0 Hex
Achimhai Medical Corporation
KMDA353570H
In Commercial Distribution

  • 08800024906836 ()


  • Dental implant suprastructure, permanent, preformed
Duplex Abutment Φ3.5/GH2.5/PH7.0 Hex
Achimhai Medical Corporation
KMDA352570H
In Commercial Distribution

  • 08800024906829 ()


  • Dental implant suprastructure, permanent, preformed
Duplex Abutment Φ3.5/GH1.5/PH7.0 Hex
Achimhai Medical Corporation
KMDA351570H
In Commercial Distribution

  • 08800024906812 ()


  • Dental implant suprastructure, permanent, preformed
Duplex Abutment Φ3.5/GH1.0/PH7.0 Hex
Achimhai Medical Corporation
KMDA351070H
In Commercial Distribution

  • 08800024906805 ()


  • Dental implant suprastructure, permanent, preformed
Duplex Abutment Φ3.5/GH4.5/PH5.5 Hex
Achimhai Medical Corporation
KMDA354555H
In Commercial Distribution

  • 08800024906799 ()


  • Dental implant suprastructure, permanent, preformed
Duplex Abutment Φ3.5/GH3.5/PH5.5 Hex
Achimhai Medical Corporation
KMDA353555H
In Commercial Distribution

  • 08800024906782 ()


  • Dental implant suprastructure, permanent, preformed
Duplex Abutment Φ3.5/GH2.5/PH5.5 Hex
Achimhai Medical Corporation
KMDA352555H
In Commercial Distribution

  • 08800024906775 ()


  • Dental implant suprastructure, permanent, preformed
Duplex Abutment Φ3.5/GH1.5/PH5.5 Hex
Achimhai Medical Corporation
KMDA351555H
In Commercial Distribution

  • 08800024906768 ()


  • Dental implant suprastructure, permanent, preformed
Duplex Abutment Φ3.5/GH1.0/PH5.5 Hex
Achimhai Medical Corporation
KMDA351055H
In Commercial Distribution

  • 08800024906751 ()


  • Dental implant suprastructure, permanent, preformed
No Description
DIO Corporation
INT 8Octa
In Commercial Distribution

  • 08800049309742 ()


  • Surgical drill guide, reusable
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