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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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OsteoStrux® Putty, 2.5cc
Seaspine Orthopedics Corporation
56070025ITL
In Commercial Distribution

  • 10889981123321 ()

  • 2.5cc
56070025ITL

  • Bone matrix implant, composite
No Description
Biomet Orthopedics, LLC
184146
In Commercial Distribution

  • 00880304435414 ()

  • 5 MM 70 MM
184146

  • Knee arthroplasty wedge
No Description
Biomet Orthopedics, LLC
184248
In Commercial Distribution

  • 00880304435407 ()

  • 10 MM 75 MM
184248

  • Knee arthroplasty wedge
IsoTis Mozaik™ Putty, 10cc
Seaspine Orthopedics Corporation
PTY10210ITL
In Commercial Distribution

  • 10889981123284 ()

  • 10cc
PTY10210ITL

  • Bone matrix implant, composite
No Description
Biomet Orthopedics, LLC
184250
In Commercial Distribution

  • 00880304435384 ()

  • 10 MM 80 MM
184250

  • Knee arthroplasty wedge
No Description
Biomet Orthopedics, LLC
184200
In Commercial Distribution

  • 00880304435377 ()

  • 10 MM 55 MM
184200

  • Knee arthroplasty wedge
No Description
Biomet Orthopedics, LLC
184206
In Commercial Distribution

  • 00880304435353 ()

  • 10 MM 70 MM
184206

  • Knee arthroplasty wedge
No Description
Biomet Orthopedics, LLC
184100
In Commercial Distribution

  • 00880304435339 ()

  • 5 MM 55 MM
184100

  • Knee arthroplasty wedge
No Description
Biomet Orthopedics, LLC
184286
In Commercial Distribution

  • 00880304435322 ()

  • 15 MM 70 MM
184286

  • Knee arthroplasty wedge
No Description
Biomet Orthopedics, LLC
184101
In Commercial Distribution

  • 00880304435254 ()

  • 5 MM 57.5 MM
184101

  • Knee arthroplasty wedge
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