SEARCH RESULTS FOR: arthrex*(17702 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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UNI GLENOID-PERIPHERAL LOCK SCRW
ARTHREX, INC.
AR-9145-36
In Commercial Distribution

  • 00888867057739 ()
  • M150AR9145361 ()
AR-9145-36

  • Shoulder glenoid fossa prosthesis, prefabricated
UNI GLENOID-PERIPHERAL LOCK SCRW
ARTHREX, INC.
AR-9145-30
In Commercial Distribution

  • 00888867057722 ()
  • M150AR9145301 ()
AR-9145-30

  • Shoulder glenoid fossa prosthesis, prefabricated
UNI GLENOID-PERIPHERAL LOCK SCRW
ARTHREX, INC.
AR-9145-24
In Commercial Distribution

  • 00888867057715 ()
  • M150AR9145241 ()
AR-9145-24

  • Shoulder glenoid fossa prosthesis, prefabricated
USP II HUMERAL HEAD 44/19
ARTHREX, INC.
AR-9144-19P
In Commercial Distribution

  • 00888867057708 ()
  • M150AR914419P1 ()
AR-9144-19P

  • Total shoulder prosthesis
USP II HUMERAL HEAD 44/17
ARTHREX, INC.
AR-9144-17P
In Commercial Distribution

  • 00888867057692 ()
  • M150AR914417P1 ()
AR-9144-17P

  • Total shoulder prosthesis
UNIVERS FRACTURE METAL HEAD, 43/15
ARTHREX, INC.
AR-9143-15F
In Commercial Distribution

  • 00888867057685 ()
  • M150AR914315F1 ()
AR-9143-15F

  • Total shoulder prosthesis
USP II HUMERAL HEAD 42/17
ARTHREX, INC.
AR-9142-17P
In Commercial Distribution

  • 00888867057678 ()
  • M150AR914217P1 ()
AR-9142-17P

  • Total shoulder prosthesis
USP II HUMERAL HEAD 40/17
ARTHREX, INC.
AR-9140-17P
In Commercial Distribution

  • 00888867057661 ()
  • M150AR914017P1 ()
AR-9140-17P

  • Total shoulder prosthesis
UNIVERSAL GLENOID CORING REAMER, LARGE
ARTHREX, INC.
AR-9127-03
In Commercial Distribution

  • 00888867057654 ()
AR-9127-03

  • Bone-resection orthopaedic reamer, reusable
UNIVERSAL GLENOID CORING REAMER, MEDIUM
ARTHREX, INC.
AR-9127-02
In Commercial Distribution

  • 00888867057647 ()
AR-9127-02

  • Bone-resection orthopaedic reamer, reusable
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