SEARCH RESULTS FOR: arthrex*(17700 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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Trial 45 / 24 Glenosphere
ARTHREX, INC.
AR-9664-2445
In Commercial Distribution

  • 00888867308947 ()
AR-9664-2445

  • Shoulder reverse/standard adaptor prosthesis trial
45mm Peripheral Reamer
ARTHREX, INC.
AR-9619-45
In Commercial Distribution

  • 00888867308930 ()
AR-9619-45

  • Bone-resection orthopaedic reamer, reusable
Inferior Glenoid Reamer 45
ARTHREX, INC.
AR-9632-45INF
In Commercial Distribution

  • 00888867308923 ()
AR-9632-45INF

  • Bone-resection orthopaedic reamer, reusable
42+6 / 45 Combination Humeral Insert
ARTHREX, INC.
AR-9503-4245-6
In Commercial Distribution

  • 00888867308916 ()
AR-9503-4245-6

  • Total reverse shoulder prosthesis
42+3 / 45 Combination Humeral Insert
ARTHREX, INC.
AR-9503-4245-3
In Commercial Distribution

  • 00888867308909 ()
AR-9503-4245-3

  • Total reverse shoulder prosthesis
39+6 / 42 Combination Humeral Insert
ARTHREX, INC.
AR-9503-3942-6
In Commercial Distribution

  • 00888867308893 ()
AR-9503-3942-6

  • Total reverse shoulder prosthesis
39+3 / 42 Combination Humeral Insert
ARTHREX, INC.
AR-9503-3942-3
In Commercial Distribution

  • 00888867308886 ()
AR-9503-3942-3

  • Total reverse shoulder prosthesis
16MM BONE DOWEL REVISION KIT
ARTHREX, INC.
ABS-2850-16
In Commercial Distribution

  • 00888867306400 ()
ABS-2850-16

  • Arthroscopic surgical procedure kit, non-medicated, single-use
14MM BONE DOWEL REVISION KIT
ARTHREX, INC.
ABS-2850-14
In Commercial Distribution

  • 00888867306394 ()
ABS-2850-14

  • Arthroscopic surgical procedure kit, non-medicated, single-use
13MM BONE DOWEL REVISION KIT
ARTHREX, INC.
ABS-2850-13
In Commercial Distribution

  • 00888867306387 ()
ABS-2850-13

  • Arthroscopic surgical procedure kit, non-medicated, single-use
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