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 Type Device Class Implantable

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Long Bullet Distractor, 18mm
SEASPINE ORTHOPEDICS CORPORATION
93-3626
In Commercial Distribution

  • 10889981089450 ()

  • 18mm
93-3626

  • Orthopaedic surgical distractor, internal
Paddle Scraper, Convex, 18mm
SEASPINE ORTHOPEDICS CORPORATION
93-3611
In Commercial Distribution

  • 10889981089337 ()

  • 18mm
93-3611

  • Bone file
Paddle Scraper, 18mm
SEASPINE ORTHOPEDICS CORPORATION
93-3488
In Commercial Distribution

  • 10889981088903 ()

  • 18mm
93-3488

  • Bone file
Paddle Distractor, Long, 18mm
SEASPINE ORTHOPEDICS CORPORATION
93-3471
In Commercial Distribution

  • 10889981088781 ()

  • 18mm
93-3471

  • Orthopaedic surgical distractor, internal
Paddle Distractor, 18mm
SEASPINE ORTHOPEDICS CORPORATION
93-3456
In Commercial Distribution

  • 10889981088668 ()

  • 18mm
93-3456

  • Orthopaedic surgical distractor, internal
Paddle Scraper, Long, Convex, 18mm
SEASPINE ORTHOPEDICS CORPORATION
93-3701
In Commercial Distribution

  • 10889981120368 ()

  • 18mm
93-3701

  • Bone file
Bullet Distractor, 18mm
SEASPINE ORTHOPEDICS CORPORATION
93-3426
In Commercial Distribution

  • 10889981120351 ()

  • 18mm
93-3426

  • Orthopaedic surgical distractor, internal
18mm Hollywood Trial, Lordotic
SEASPINE ORTHOPEDICS CORPORATION
93-4188
In Commercial Distribution

  • 10889981058425 ()

  • 18mm
93-4188

  • Spinal implant trial
18mm Long Ventura Trial
SEASPINE ORTHOPEDICS CORPORATION
93-3386
In Commercial Distribution

  • 10889981033415 ()

  • 18mm
93-3386

  • Spinal implant trial
18mm Hollywood Trial, Lordotic
SEASPINE ORTHOPEDICS CORPORATION
93-4261
In Commercial Distribution

  • 10889981031305 ()

  • 18mm
93-4261

  • Spinal implant trial
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