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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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Lordotic Scoring Trial, 6 mm x 15.5 mm x 14 mm
Spine Wave, Inc.
10-5610
In Commercial Distribution

  • 10840642120929 ()
10-5610

  • Polymeric spinal interbody fusion cage
Lordotic Scoring Trial, 5 mm x 15.5 mm x 14 mm
Spine Wave, Inc.
10-5609
In Commercial Distribution

  • 10840642120912 ()
10-5609

  • Polymeric spinal interbody fusion cage
Cannulated, Extended Tab Screw, 4.2 mm X 50 mm
Spine Wave, Inc.
21-8454
In Commercial Distribution

  • 10840642120905 ()
21-8454

  • Spinal bone screw, non-bioabsorbable
Cannulated, Extended Tab Screw, 4.2 mm X 48 mm
Spine Wave, Inc.
21-8453
In Commercial Distribution

  • 10840642120899 ()
21-8453

  • Spinal bone screw, non-bioabsorbable
Cannulated, Extended Tab Screw, 4.2 mm X 46 mm
Spine Wave, Inc.
21-8452
In Commercial Distribution

  • 10840642120882 ()
21-8452

  • Spinal bone screw, non-bioabsorbable
Cannulated, Extended Tab Screw, 4.2 mm X 45 mm
Spine Wave, Inc.
21-8451
In Commercial Distribution

  • 10840642120875 ()
21-8451

  • Spinal bone screw, non-bioabsorbable
Cannulated, Extended Tab Screw, 4.2 mm X 44 mm
Spine Wave, Inc.
21-8450
In Commercial Distribution

  • 10840642120868 ()
21-8450

  • Spinal bone screw, non-bioabsorbable
Cannulated, Extended Tab Screw, 4.2 mm X 42 mm
Spine Wave, Inc.
21-8449
In Commercial Distribution

  • 10840642120851 ()
21-8449

  • Spinal bone screw, non-bioabsorbable
Cannulated, Extended Tab Screw, 4.2 mm X 40 mm
Spine Wave, Inc.
21-8448
In Commercial Distribution

  • 10840642120844 ()
21-8448

  • Spinal bone screw, non-bioabsorbable
Cannulated, Extended Tab Screw, 4.2 mm X 38 mm
Spine Wave, Inc.
21-8447
In Commercial Distribution

  • 10840642120837 ()
21-8447

  • Spinal bone screw, non-bioabsorbable
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