SEARCH RESULTS FOR: arthrex*(8149 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 Class Implantable

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Arthroscopy Instrument Case
ARTHREX, INC.
AR-8656C
In Commercial Distribution

  • 00888867346062 ()
AR-8656C

  • Device sterilization/disinfection container, reusable
GraftClamp, Graft Preparation Instrument
ARTHREX, INC.
AR-2386T
In Commercial Distribution

  • 00888867345898 ()
AR-2386T

  • Orthopaedic implant/instrument assembling device
Synergy Shaver & Power™ Console
ARTHREX, INC.
AR-S8307
In Commercial Distribution

  • 00888867345881 ()
AR-S8307

  • Arthroscopic shaver system, electrically-powered
DualComp Hindfoot Fusion, Screw Caddy
ARTHREX, INC.
AR-9090C-SC-01
In Commercial Distribution

  • 00888867345850 ()
AR-9090C-SC-01

  • Device sterilization/disinfection container, reusable
DualComp Hindfoot Fusion System, Case
ARTHREX, INC.
AR-9090C
In Commercial Distribution

  • 00888867345843 ()
AR-9090C

  • Device sterilization/disinfection container, reusable
Drill Guide, 2.0mm / 2.5mm
ARTHREX, INC.
AR-9944-05
In Commercial Distribution

  • 00888867345799 ()
AR-9944-05

  • Surgical drill guide, reusable
Drill Guide, MaxForce MTP Comp Device
ARTHREX, INC.
AR-9944-04
In Commercial Distribution

  • 00888867345782 ()
AR-9944-04

  • Surgical drill guide, reusable
24MM BASEPLATE, 20° FULL AUGMENT TRIAL
ARTHREX, INC.
AR-9594-2420
In Commercial Distribution

  • 00888867343818 ()
AR-9594-2420

  • Shoulder glenoid fossa prosthesis trial
24MM BASEPLATE, 10° FULL AUGMENT TRIAL
ARTHREX, INC.
AR-9594-2410
In Commercial Distribution

  • 00888867343801 ()
AR-9594-2410

  • Shoulder glenoid fossa prosthesis trial
28MM BASEPLATE, 35° HALF AUGMENT TRIAL
ARTHREX, INC.
AR-9593-2835
In Commercial Distribution

  • 00888867343795 ()
AR-9593-2835

  • Shoulder glenoid fossa prosthesis trial
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