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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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BONE FILE #21 SINGLE CUT HD D/E - D928105221HD0

No Description
W.H. Holden, Inc.
10-5221HD
In Commercial Distribution

  • D928105221HD0 ()


  • Bone file/rasp, reciprocating, single-use

BONE FILE #12 SINGLE CUT HD D/E - D928105212HD0

No Description
W.H. Holden, Inc.
10-5212HD
In Commercial Distribution

  • D928105212HD0 ()


  • Bone file/rasp, reciprocating, single-use

PA TUNNELING INSTRUMENT #4 D/E HF HANDLE - D928400533HF0

No Description
W.H. Holden, Inc.
40-0533HF
In Commercial Distribution

  • D928400533HF0 ()


  • Periodontal knife

PA TUNNELING INSTRUMENT #3 D/E HF HANDLE - D928400532HF0

No Description
W.H. Holden, Inc.
40-0532HF
In Commercial Distribution

  • D928400532HF0 ()


  • Periodontal knife

PA TUNNELING INSTRUMENT #2 D/E HF HANDLE - D928400531HF0

No Description
W.H. Holden, Inc.
40-0531HF
In Commercial Distribution

  • D928400531HF0 ()


  • Periodontal knife

CURETTE MOLT 2/4HD ANGLED HF D/E - D9281051062HF0

No Description
W.H. Holden, Inc.
10-5106-2HF
In Commercial Distribution

  • D9281051062HF0 ()


  • Bone curette, reusable

CURETTE MOLT 2/4HD ANGLED HD D/E - D9281051062HD0

No Description
W.H. Holden, Inc.
10-5106-2HD
In Commercial Distribution

  • D9281051062HD0 ()


  • Bone curette, reusable

CURETTE MOLT 2/4HD ANGLED HF D/E - D9281051061HF0

No Description
W.H. Holden, Inc.
10-5106-1HF
In Commercial Distribution

  • D9281051061HF0 ()


  • Bone curette, reusable

ROOT ELEVATOR APICAL #2 HD S/E SERRATED - D928105036HD20

No Description
W.H. Holden, Inc.
10-5036HD2
In Commercial Distribution

  • D928105036HD20 ()


  • Dental elevator, tooth/root

ROOT ELEVATOR APICAL #1 HD S/E SERRATED - D928105036HD10

No Description
W.H. Holden, Inc.
10-5036HD1
In Commercial Distribution

  • D928105036HD10 ()


  • Dental elevator, tooth/root
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