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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 - 10840843104995

No Description
GLOBUS MEDICAL, INC.
SC2265-5-12
In Commercial Distribution

  • 10840843104995 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104971

No Description
GLOBUS MEDICAL, INC.
SC2265-4-30
In Commercial Distribution

  • 10840843104971 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104964

No Description
GLOBUS MEDICAL, INC.
SC2265-4-26
In Commercial Distribution

  • 10840843104964 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104940

No Description
GLOBUS MEDICAL, INC.
SC2265-4-20
In Commercial Distribution

  • 10840843104940 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104926

No Description
GLOBUS MEDICAL, INC.
SC2265-4-14
In Commercial Distribution

  • 10840843104926 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104902

No Description
GLOBUS MEDICAL, INC.
SC2265-4-10
In Commercial Distribution

  • 10840843104902 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104889

No Description
GLOBUS MEDICAL, INC.
SC2265-3-26
In Commercial Distribution

  • 10840843104889 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104858

No Description
GLOBUS MEDICAL, INC.
SC2265-3-17
In Commercial Distribution

  • 10840843104858 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104841

No Description
GLOBUS MEDICAL, INC.
SC2265-3-14
In Commercial Distribution

  • 10840843104841 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843104827

No Description
GLOBUS MEDICAL, INC.
SC2265-3-10
In Commercial Distribution

  • 10840843104827 ()


  • Tibial insert
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