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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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Spand-Gel Hydrogel Wound Filler Bellows Bottle 1oz
MEDI-TECH INTERNATIONAL CORPORATION
SPHD01
In Commercial Distribution

  • 00027479260018 ()
SPHD01

  • Wound hydrogel dressing, non-sterile
Zinc Wound Wash First Aid Cleanser
WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
311263
In Commercial Distribution

  • 00050428287071 ()

  • Total Volume: 4 Fluid Ounce
  • Total Volume: 118 Milliliter
311263

  • Non-antimicrobial wound irrigation solution, multiple solute, sterile
Sponges Non Woven Non Sterile 4" x 4" 4Ply 2,000/cs - MARK3
CARGUS INTERNATIONAL, INC
2226
In Commercial Distribution

  • D79622261 ()


  • Non-woven gauze pad, non-sterile
Sponges Non Woven Non Sterile 2" x 2" 4Ply 5000/cs. - MARK3
CARGUS INTERNATIONAL, INC
2224
In Commercial Distribution

  • D79622241 ()


  • Non-woven gauze pad, non-sterile
Foaming Dual Enzymatic Spray
METREX RESEARCH, LLC
10-4224
In Commercial Distribution

  • H97110422424 ()
  • 00615375005606 ()

  • Total Volume: 24 Fluid Ounce


  • Medical device-decontamination agent
The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical rasps are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm.
BLUSTONE SYNERGY, LLC
9017-CRP9
In Commercial Distribution

  • 00810482031238 ()

  • Width: 13 Millimeter
  • Height: 9 Millimeter
  • Length: 17 Millimeter


  • Bone file
The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical rasps are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm.
BLUSTONE SYNERGY, LLC
9017-CRP8
In Commercial Distribution

  • 00810482031221 ()

  • Width: 13 Millimeter
  • Height: 8 Millimeter
  • Length: 17 Millimeter


  • Bone file
The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical rasps are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm.
BLUSTONE SYNERGY, LLC
9017-CRP7
In Commercial Distribution

  • 00810482031214 ()

  • Width: 13 Millimeter
  • Height: 7 Millimeter
  • Length: 17 Millimeter


  • Bone file
The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical rasps are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm.
BLUSTONE SYNERGY, LLC
9017-CRP6
In Commercial Distribution

  • 00810482031207 ()

  • Width: 13 Millimeter
  • Height: 6 Millimeter
  • Length: 17 Millimeter


  • Bone file
The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical rasps are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm.
BLUSTONE SYNERGY, LLC
9017-CRP5
In Commercial Distribution

  • 00810482031191 ()

  • Width: 13 Millimeter
  • Height: 5 Millimeter
  • Length: 17 Millimeter


  • Bone file
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