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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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BLUNT BLADE, 20 X 60 MM, GOLD
TEDAN SURGICAL INNOVATIONS, L.L.C.
CS-0036
In Commercial Distribution

  • 00843059105216 ()


  • Surgical retractor/retraction system blade, reusable
BLUNT BLADE, 20 X 55 MM, BLACK
TEDAN SURGICAL INNOVATIONS, L.L.C.
CS-0035
In Commercial Distribution

  • 00843059105209 ()


  • Surgical retractor/retraction system blade, reusable
BLUNT BLADE, 20 X 50 MM, PURPLE
TEDAN SURGICAL INNOVATIONS, L.L.C.
CS-0034
In Commercial Distribution

  • 00843059105193 ()


  • Surgical retractor/retraction system blade, reusable
BLUNT BLADE, 20 X 45 MM, GREEN
TEDAN SURGICAL INNOVATIONS, L.L.C.
CS-0033
In Commercial Distribution

  • 00843059105186 ()


  • Surgical retractor/retraction system blade, reusable
BLUNT BLADE, 20 X 40 MM, RED
TEDAN SURGICAL INNOVATIONS, L.L.C.
CS-0032
In Commercial Distribution

  • 00843059105179 ()


  • Surgical retractor/retraction system blade, reusable
BLUNT BLADE, 20 X 35 MM, BLUE
TEDAN SURGICAL INNOVATIONS, L.L.C.
CS-0031
In Commercial Distribution

  • 00843059105162 ()


  • Surgical retractor/retraction system blade, reusable
BLUNT BLADE, 20 X 30 MM, SILVER
TEDAN SURGICAL INNOVATIONS, L.L.C.
CS-0030
In Commercial Distribution

  • 00843059105155 ()


  • Surgical retractor/retraction system blade, reusable
PEEK/Titanium Interbody, 20 °, 42mm x 30mm
Altus Spine, LLC
SL42302020
In Commercial Distribution

  • 00843210159966 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 42mm x 30mm
Altus Spine, LLC
SL42302019
In Commercial Distribution

  • 00843210159959 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 42mm x 30mm
Altus Spine, LLC
SL42302018
In Commercial Distribution

  • 00843210159942 ()


  • Polymeric spinal interbody fusion cage
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