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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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Insignia - 00190376274713

20° Trial Drill Guide, 10mm
ALPHATEC SPINE, INC.
137-22010
In Commercial Distribution

  • 00190376274713 ()


  • Surgical drill guide, reusable

Insignia - 00190376274690

20° Trial Drill Guide, 8mm
ALPHATEC SPINE, INC.
137-22008
In Commercial Distribution

  • 00190376274690 ()


  • Surgical drill guide, reusable

Insignia - 00190376274676

20° Trial Drill Guide, 6mm
ALPHATEC SPINE, INC.
137-22006
In Commercial Distribution

  • 00190376274676 ()


  • Surgical drill guide, reusable

Insignia - 00190376274737

20° Trial Drill Guide, 12mm
ALPHATEC SPINE, INC.
137-22012
In Commercial Distribution

  • 00190376274737 ()


  • Surgical drill guide, reusable

Insignia - 00190376274720

20° Trial Drill Guide, 11mm
ALPHATEC SPINE, INC.
137-22011
In Commercial Distribution

  • 00190376274720 ()


  • Surgical drill guide, reusable

Insignia - 00190376274706

20° Trial Drill Guide, 9mm
ALPHATEC SPINE, INC.
137-22009
In Commercial Distribution

  • 00190376274706 ()


  • Surgical drill guide, reusable

Insignia - 00190376274683

20° Trial Drill Guide, 7mm
ALPHATEC SPINE, INC.
137-22007
In Commercial Distribution

  • 00190376274683 ()


  • Surgical drill guide, reusable

Insignia - 00190376274669

20° Trial Drill Guide, 5mm
ALPHATEC SPINE, INC.
137-22005
In Commercial Distribution

  • 00190376274669 ()


  • Surgical drill guide, reusable

Insignia - 00190376268460

Insignia, ACP, 1-Level, 20 mm
ALPHATEC SPINE, INC.
136-0120
Not in Commercial Distribution

  • 00190376268460 ()


  • Spinal fixation plate, non-bioabsorbable

Spark - 00889989084825

Spark 20 / Active - Single Arch
ORMCO CORPORATION
728-3021
In Commercial Distribution

  • 00889989084825 ()


  • Orthodontic progressive aligner
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