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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Extension Aligner
SEASPINE ORTHOPEDICS CORPORATION
28-40-0034
In Commercial Distribution

  • 10889981116972 ()
28-40-0034

  • Orthopaedic implant-instrument extension adaptor, reusable
Radel Dilator Stage #4
SEASPINE ORTHOPEDICS CORPORATION
28-40-0023
In Commercial Distribution

  • 10889981116859 ()
28-40-0023

  • Orthopaedic retractor
Dilator Stage #3
SEASPINE ORTHOPEDICS CORPORATION
28-40-0022
In Commercial Distribution

  • 10889981116842 ()
28-40-0022

  • Orthopaedic retractor
Dilator Stage #2
SEASPINE ORTHOPEDICS CORPORATION
28-40-0021
In Commercial Distribution

  • 10889981116835 ()
28-40-0021

  • Orthopaedic retractor
Dilator Stage #1
SEASPINE ORTHOPEDICS CORPORATION
28-40-0020
In Commercial Distribution

  • 10889981116828 ()
28-40-0020

  • Orthopaedic retractor
K-Wire, Threaded, Nitinol, 680
SEASPINE ORTHOPEDICS CORPORATION
28-40-0019-680
In Commercial Distribution

  • 10889981116811 ()

  • 680
28-40-0019-680

  • Catheter stylet
K-Wire, Threaded, Nitinol, 500
SEASPINE ORTHOPEDICS CORPORATION
28-40-0019-500
In Commercial Distribution

  • 10889981116804 ()

  • 500
28-40-0019-500

  • Catheter stylet
K-Wire, Threaded, Nitinol, 380
SEASPINE ORTHOPEDICS CORPORATION
28-40-0019-380
In Commercial Distribution

  • 10889981116798 ()

  • 380
28-40-0019-380

  • Catheter stylet
K-Wire, Blunt, Nitinol, 680
SEASPINE ORTHOPEDICS CORPORATION
28-40-0018-680
In Commercial Distribution

  • 10889981116781 ()

  • 680
28-40-0018-680

  • Catheter stylet
K-Wire, Blunt, Nitinol, 500
SEASPINE ORTHOPEDICS CORPORATION
28-40-0018-500
In Commercial Distribution

  • 10889981116774 ()

  • 500
28-40-0018-500

  • Catheter stylet
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