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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 CR HF Knee System - 10840843107750

No Description
GLOBUS MEDICAL, INC.
SC2829-2.5-12
In Commercial Distribution

  • 10840843107750 ()


  • Tibial insert

Proven Gen-Flex CR HF Knee System - 10840843107712

No Description
GLOBUS MEDICAL, INC.
SC2829-1-23
In Commercial Distribution

  • 10840843107712 ()


  • Tibial insert

Proven Gen-Flex CR HF Knee System - 10840843107699

No Description
GLOBUS MEDICAL, INC.
SC2829-1-17
In Commercial Distribution

  • 10840843107699 ()


  • Tibial insert

Proven Gen-Flex CR HF Knee System - 10840843107675

No Description
GLOBUS MEDICAL, INC.
SC2829-1-12
In Commercial Distribution

  • 10840843107675 ()


  • Tibial insert

Proven Gen-Flex Modular/Revision Knee System - 10840843105022

No Description
GLOBUS MEDICAL, INC.
SC2265-5-20
In Commercial Distribution

  • 10840843105022 ()


  • Tibial insert

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 - 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
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