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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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TLX - 00887517825155

TLX Implant, 12x11x26mm 20°
Nuvasive, Inc.
1792626
In Commercial Distribution

  • 00887517825155 ()


  • Metallic spinal interbody fusion cage

TLX - 00887517825070

TLX Implant, 10x11x31mm 20°
Nuvasive, Inc.
1792618
In Commercial Distribution

  • 00887517825070 ()


  • Metallic spinal interbody fusion cage

TLX - 00887517825056

TLX Implant, 10x11x26mm 20°
Nuvasive, Inc.
1792616
In Commercial Distribution

  • 00887517825056 ()


  • Metallic spinal interbody fusion cage

TLX - 00887517824974

TLX Implant, 8x11x31mm 20°
Nuvasive, Inc.
1792608
In Commercial Distribution

  • 00887517824974 ()


  • Metallic spinal interbody fusion cage

TLX - 00887517824950

TLX Implant, 8x11x26mm 20°
Nuvasive, Inc.
1792606
In Commercial Distribution

  • 00887517824950 ()


  • Metallic spinal interbody fusion cage

TLX - 00887517824905

TLX Implant, 7x11x26mm 20°
Nuvasive, Inc.
1792601
In Commercial Distribution

  • 00887517824905 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517811875

Interlock II, 16x19x16mm 20°
Nuvasive, Inc.
6779620
In Commercial Distribution

  • 00887517811875 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517811752

Interlock II, 15x19x16mm 20°
Nuvasive, Inc.
6779520
In Commercial Distribution

  • 00887517811752 ()


  • Polymeric spinal interbody fusion cage

Halyard - 30680651793561

HYH,OPTH,DRAPE,-,-,20
O&M HALYARD, INC.
79356
In Commercial Distribution

  • 30680651793561 ()
  • 90680651793563 ()


  • Patient surgical drape, single-use, non-sterile

Halyard - 30680651006890

HYH ACM,-,SHTTPE,-,-,20
O&M HALYARD, INC.
00689
In Commercial Distribution

  • 30680651006890 ()
  • 90680651006892 ()
ACM0689

  • Patient surgical drape, single-use, non-sterile
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