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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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PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242014
In Commercial Distribution

  • 00843210188034 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242013
In Commercial Distribution

  • 00843210188027 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242012
In Commercial Distribution

  • 00843210188010 ()


  • Polymeric spinal interbody fusion cage
20 ParaPost XP Titanium Temp Posts - .070
COLTENE/WHALEDENT INC
P7467
In Commercial Distribution

  • D661P74671 ()
  • D661P74670 ()


  • Root canal post, preformed
20 ParaPost XP Titanium Temp Posts - .060
COLTENE/WHALEDENT INC
P7466
In Commercial Distribution

  • D661P74661 ()
  • D661P74660 ()


  • Root canal post, preformed
20 ParaPost XP Titanium Temp Posts - .055
COLTENE/WHALEDENT INC
P74655
In Commercial Distribution

  • D661P746551 ()
  • D661P746550 ()


  • Root canal post, preformed
20 ParaPost XP Titanium Temp Posts - .050
COLTENE/WHALEDENT INC
P7465
In Commercial Distribution

  • D661P74651 ()
  • D661P74650 ()


  • Root canal post, preformed
20 ParaPost XP Titanium Temp Posts - .045
COLTENE/WHALEDENT INC
P74645
In Commercial Distribution

  • D661P746451 ()
  • D661P746450 ()


  • Root canal post, preformed
20 ParaPost XP Titanium Temp Posts - .040
COLTENE/WHALEDENT INC
P7464
In Commercial Distribution

  • D661P74641 ()
  • D661P74640 ()


  • Root canal post, preformed
20 ParaPost XP Titanium Temp Posts - .036
COLTENE/WHALEDENT INC
P7463
In Commercial Distribution

  • D661P74631 ()
  • D661P74630 ()


  • Root canal post, preformed
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