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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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REVERS GLENOID POROUS COAT- BASEPLATE, M
ARTHREX, INC.
AR-9120-02PC
In Commercial Distribution

  • 00888867286566 ()
AR-9120-02PC

  • Shoulder glenoid fossa prosthesis, prefabricated
SutureTape, 1.3mm w/Needle, White/Blue
ARTHREX, INC.
AR-7500-1
In Commercial Distribution

  • 00888867286542 ()
AR-7500-1

  • Polyolefin/fluoropolymer suture, multifilament
TigerLink, 0, white/black
ARTHREX, INC.
AR-7258T-1
In Commercial Distribution

  • 00888867286498 ()
AR-7258T-1

  • Polyolefin/fluoropolymer suture, multifilament
FiberLink 0, blue
ARTHREX, INC.
AR-7258-1
In Commercial Distribution

  • 00888867286481 ()
AR-7258-1

  • Polyolefin/fluoropolymer suture, multifilament
FIBERTAPE, 17" W/ STR NDL
ARTHREX, INC.
AR-7237-17LN-1
In Commercial Distribution

  • 00888867286429 ()
AR-7237-17LN-1

  • Polyolefin/fluoropolymer suture, multifilament
FiberLoop, 2-0, Looped w/ Curved Ndle
ARTHREX, INC.
AR-7232-05-1
In Commercial Distribution

  • 00888867286412 ()
AR-7232-05-1

  • Polyolefin/fluoropolymer suture, multifilament
4-0 FIBERLOOP, 20 INCHES WITH NEEDLE
ARTHREX, INC.
AR-7229-20-1
In Commercial Distribution

  • 00888867286399 ()
AR-7229-20-1

  • Polyolefin/fluoropolymer suture, multifilament
#4-0 FW,BRAID POLYBLEND SUTR 18" BLU
ARTHREX, INC.
AR-7228-1
In Commercial Distribution

  • 00888867286382 ()
AR-7228-1

  • Polyolefin/fluoropolymer suture, multifilament
PEEK PushLock Tenodesis, Closed Eyelet
ARTHREX, INC.
AR-1663PC-8
In Commercial Distribution

  • 10888867286068 ()
  • 00888867286061 ()
AR-1663PC-8

  • Tendon/ligament bone anchor, non-bioabsorbable
SUTURE ANCHOR, PEEK CORKSCREW FT
ARTHREX, INC.
AR-1927PSF-65-1
In Commercial Distribution

  • 00888867285828 ()
AR-1927PSF-65-1

  • Tendon/ligament bone anchor, non-bioabsorbable
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