SEARCH RESULTS FOR: seaspine(25470 results)

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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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Cup-#3 Left 30 Deg Bayonetted
Seaspine Orthopedics Corporation
06-50-0112
In Commercial Distribution

  • 10889981104214 ()

  • 30 Deg
06-50-0112

  • Bone curette, reusable
Cup-#3 Right 30 Deg Bayonetted
Seaspine Orthopedics Corporation
06-50-0111
In Commercial Distribution

  • 10889981104207 ()

  • 30 Deg
06-50-0111

  • Bone curette, reusable
Cup-#3 Fwd Bayonetted
Seaspine Orthopedics Corporation
06-50-0110
In Commercial Distribution

  • 10889981104191 ()
06-50-0110

  • Bone curette, reusable
Curette-#1 Pull Rev Bayonetted
Seaspine Orthopedics Corporation
06-50-0104
In Commercial Distribution

  • 10889981104184 ()
06-50-0104

  • Bone curette, reusable
Curette- #1 Left 30 Deg Bayonetted
Seaspine Orthopedics Corporation
06-50-0102
In Commercial Distribution

  • 10889981104160 ()

  • 30 Deg
06-50-0102

  • Bone curette, reusable
Curette-#1 Right 30 Deg Bayonetted
Seaspine Orthopedics Corporation
06-50-0101
In Commercial Distribution

  • 10889981104153 ()

  • 30 Deg
06-50-0101

  • Bone curette, reusable
Cup-#0 Pull Rev Bayonetted
Seaspine Orthopedics Corporation
06-50-0092
In Commercial Distribution

  • 10889981104139 ()
06-50-0092

  • Bone curette, reusable
Cup-#0 Pull Fwd Bayonetted
Seaspine Orthopedics Corporation
06-50-0091
In Commercial Distribution

  • 10889981104122 ()
06-50-0091

  • Bone curette, reusable
Curette-#4/0 Pull Rev Bayonetted
Seaspine Orthopedics Corporation
06-50-0082
In Commercial Distribution

  • 10889981104108 ()
06-50-0082

  • Bone curette, reusable
Retractor-Nerve Root 90 Deg Wide
Seaspine Orthopedics Corporation
06-50-0060
In Commercial Distribution

  • 10889981104054 ()

  • 90 Deg
06-50-0060

  • Orthopaedic retractor
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