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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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TO BE ASSIGNED - 00193033522691

No Description
FGX INTERNATIONAL INC.
10262918.INT
In Commercial Distribution

  • 00193033522691 ()


  • Tinted non-prescription spectacles

TO BE ASSIGNED - 00193033518182

No Description
FGX INTERNATIONAL INC.
5013887-350.INT
In Commercial Distribution

  • 00193033518182 ()


  • Prescription spectacles

TO BE ASSIGNED - 00193033518175

No Description
FGX INTERNATIONAL INC.
5013887-300.INT
In Commercial Distribution

  • 00193033518175 ()


  • Prescription spectacles

TO BE ASSIGNED - 00193033518168

No Description
FGX INTERNATIONAL INC.
5013887-250.INT
In Commercial Distribution

  • 00193033518168 ()


  • Prescription spectacles

TO BE ASSIGNED - 00193033518151

No Description
FGX INTERNATIONAL INC.
5013887-200.INT
In Commercial Distribution

  • 00193033518151 ()


  • Prescription spectacles

TO BE ASSIGNED - 00193033518144

No Description
FGX INTERNATIONAL INC.
5013887-150.INT
In Commercial Distribution

  • 00193033518144 ()


  • Prescription spectacles

TO BE ASSIGNED - 00193033518137

No Description
FGX INTERNATIONAL INC.
5013887-100.INT
In Commercial Distribution

  • 00193033518137 ()


  • Prescription spectacles

TO BE ASSIGNED - 00999999005977

No Description
FGX INTERNATIONAL INC.
3865003.LTS
Not in Commercial Distribution

  • 00999999005977 ()


  • Prescription spectacles

ENDOSKELETON® TO - 00191375052531

Modular Head Trial Remover
MEDTRONIC SOFAMOR DANEK, INC.
1000-0211
In Commercial Distribution

  • 00191375052531 ()


  • Orthopaedic inorganic implant inserter/extractor, reusable

ENDOSKELETON® TO - 00191375052111

Caddy, Base
MEDTRONIC SOFAMOR DANEK, INC.
920-042-002
In Commercial Distribution

  • 00191375052111 ()


  • Instrument tray, reusable
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