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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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Proven Gen-Flex Modular/Revision Knee System - 10840843104810

No Description
GLOBUS MEDICAL, INC.
SC2265-2-30
In Commercial Distribution

  • 10840843104810 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104780

No Description
GLOBUS MEDICAL, INC.
SC2265-2-20
In Commercial Distribution

  • 10840843104780 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104773

No Description
GLOBUS MEDICAL, INC.
SC2265-2-17
In Commercial Distribution

  • 10840843104773 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104759

No Description
GLOBUS MEDICAL, INC.
SC2265-2-12
In Commercial Distribution

  • 10840843104759 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104735

No Description
GLOBUS MEDICAL, INC.
SC2265-1-30
In Commercial Distribution

  • 10840843104735 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104711

No Description
GLOBUS MEDICAL, INC.
SC2265-1-23
In Commercial Distribution

  • 10840843104711 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104698

No Description
GLOBUS MEDICAL, INC.
SC2265-1-17
In Commercial Distribution

  • 10840843104698 ()


  • Tibial insert

Proven Gen-Flex CR Knee System - 10840843103745

No Description
GLOBUS MEDICAL, INC.
SC2045-6-23
Not in Commercial Distribution

  • 10840843103745 ()


  • Tibial insert

Proven Gen-Flex CR Knee System - 10840843103721

No Description
GLOBUS MEDICAL, INC.
SC2045-6-17
Not in Commercial Distribution

  • 10840843103721 ()


  • Tibial insert

Proven Gen-Flex CR Knee System - 10840843103691

No Description
GLOBUS MEDICAL, INC.
SC2045-6-10
Not in Commercial Distribution

  • 10840843103691 ()


  • Tibial insert
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