SEARCH RESULTS FOR: Femoral(87343 results)

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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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Femoral Augment Posterior, Size 5+, 5mm
Omni Life Science, Inc.
KP-45050
In Commercial Distribution

  • 00841690126300 ()
KP-45050

  • Knee arthroplasty wedge
Femoral Augment Posterior, Size 4+, 10mm
Omni Life Science, Inc.
KP-44100
In Commercial Distribution

  • 00841690125181 ()
KP-44100

  • Knee arthroplasty wedge
Femoral Augment Posterior, Size 4+, 5mm
Omni Life Science, Inc.
KP-44050
In Commercial Distribution

  • 00841690125150 ()
KP-44050

  • Knee arthroplasty wedge
Femoral Augment Posterior, Size 3+, 10mm
Omni Life Science, Inc.
KP-43100
In Commercial Distribution

  • 00841690121404 ()
KP-43100

  • Knee arthroplasty wedge
Femoral Augment Posterior, Size 3+, 5mm
Omni Life Science, Inc.
KP-43050
In Commercial Distribution

  • 00841690121374 ()
KP-43050

  • Knee arthroplasty wedge
Femoral Augment Posterior, Size 2+, 10mm
Omni Life Science, Inc.
KP-42100
In Commercial Distribution

  • 00841690121343 ()
KP-42100

  • Knee arthroplasty wedge
Femoral Augment Posterior, Size 2+, 5mm
Omni Life Science, Inc.
KP-42050
In Commercial Distribution

  • 00841690121312 ()
KP-42050

  • Knee arthroplasty wedge
Femoral Augment Posterior, Size 1+, 10mm
Omni Life Science, Inc.
KP-41100
In Commercial Distribution

  • 00841690121282 ()
KP-41100

  • Knee arthroplasty wedge
Femoral Augment Posterior, Size 1+, 5mm
Omni Life Science, Inc.
KP-41050
In Commercial Distribution

  • 00841690121251 ()
KP-41050

  • Knee arthroplasty wedge
CR Femoral Trial Size 6 Left
Omni Life Science, Inc.
KS-1460L
In Commercial Distribution

  • 00841690121114 ()
KS-1460L

  • Knee femur prosthesis trial, reusable
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