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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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BONE AWL
SpineArt SA
ELL-IN 02 01-N
In Commercial Distribution

  • 07640139349781 ()
ELL-IN 02 01-N

  • Bone awl, reusable
SETSCREW TUBE
SpineArt SA
ELL-IN 01 15-N
In Commercial Distribution

  • 07640139349774 ()
ELL-IN 01 15-N

  • Orthopaedic implantation sleeve, reusable
Setscrew holder
SpineArt SA
ELL-IN 01 10-N
In Commercial Distribution

  • 07640139349750 ()
ELL-IN 01 10-N

  • General internal orthopaedic fixation system implantation kit
STRAIGHT ENDTIP
SpineArt SA
ELL-IN 02 08-N
In Commercial Distribution

  • 07640139349743 ()
ELL-IN 02 08-N

  • Orthopaedic surgical distractor, internal
PEDICLE SOUNDER
SpineArt SA
ELL-IN 01 02-N
In Commercial Distribution

  • 07640139349736 ()
ELL-IN 01 02-N

  • Abdominal/ENT/orthopaedic surgical probe, reusable
HOOK PUSHER
SpineArt SA
ELL-IN 00 32-N
In Commercial Distribution

  • 07640139349712 ()
ELL-IN 00 32-N

  • Orthopaedic inorganic implant inserter/extractor, reusable
STABILIZER
SpineArt SA
MIS-IN 29 00-N
In Commercial Distribution

  • 07640139349514 ()
MIS-IN 29 00-N

  • Orthopaedic rod reducer
UNIVERSAL TUBE
SpineArt SA
MIS-IN 28 01-N
In Commercial Distribution

  • 07640139349507 ()
MIS-IN 28 01-N

  • Orthopaedic rod reducer
RELEASE TUBE
SpineArt SA
MIS-IN 26 00-N
In Commercial Distribution

  • 07640139349491 ()
MIS-IN 26 00-N

  • Surgical instrument handle, non-torque-limiting
PERSUADER
SpineArt SA
MIS-IN 21 00-N
In Commercial Distribution

  • 07640139349484 ()
MIS-IN 21 00-N

  • Orthopaedic rod reducer
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