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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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Intervertebral Disc Preparation Instruments - 00190376394350

LIF, RASP, CC OFFSET, 10MM
ALPHATEC SPINE, INC.
256-16-100-10
In Commercial Distribution

  • 00190376394350 ()


  • Bone file/rasp, manual, reusable

Intervertebral Disc Preparation Instruments - 00190376393223

LIF, RASP, CC OFFSET, 24MM
ALPHATEC SPINE, INC.
256-16-100-24
In Commercial Distribution

  • 00190376393223 ()


  • Bone file/rasp, manual, reusable

Hero - 00840606104135

HERO DBM+ PASTE, 8 CC
SPINAL ELEMENTS, INC.
01002-008
In Commercial Distribution

  • 00840606104135 ()


  • Bone matrix implant, human-derived

Hero - 00840606104128

HERO DBM+ PASTE, 3 CC
SPINAL ELEMENTS, INC.
01002-003
In Commercial Distribution

  • 00840606104128 ()


  • Bone matrix implant, human-derived

Hero - 00840606104111

HERO DBM+ PASTE, 1 CC
SPINAL ELEMENTS, INC.
01002-001
In Commercial Distribution

  • 00840606104111 ()


  • Bone matrix implant, human-derived

Hero - 00840606104104

HERO DBM PUTTY, 10 CC
SPINAL ELEMENTS, INC.
01001-010
In Commercial Distribution

  • 00840606104104 ()


  • Bone matrix implant, human-derived

Hero - 00840606104098

HERO DBM PUTTY, 5 CC
SPINAL ELEMENTS, INC.
01001-005
In Commercial Distribution

  • 00840606104098 ()


  • Bone matrix implant, human-derived

Hero - 00840606104081

HERO DBM PUTTY, 2.5 CC
SPINAL ELEMENTS, INC.
01001-002
In Commercial Distribution

  • 00840606104081 ()


  • Bone matrix implant, human-derived

Hero - 00840606104074

HERO DBM PUTTY, 1 CC
SPINAL ELEMENTS, INC.
01001-001
In Commercial Distribution

  • 00840606104074 ()


  • Bone matrix implant, human-derived

Millennium - 00190776197834

Standard Single Port cc Toomey
Avalign Technologies, Inc.
39-CA3STD4.630TMY
In Commercial Distribution

  • 00190776197834 ()


  • Liposuction system cannula, reusable
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