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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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.016 X .022 UPPER HEAT ACTIVATED NITINOL WITH DIMPLE RIGHT FORM (10)
Ortho Arch Company Inc
226-512
In Commercial Distribution

  • D90922651215 ()
226-512

  • Orthodontic archwire
.016 X .016 LOWER HEAT ACTIVATED NITINOL WITH DIMPLE RIGHT FORM (10)
Ortho Arch Company Inc
226-511
In Commercial Distribution

  • D90922651114 ()
226-511

  • Orthodontic archwire
.020 UPPER HEAT ACTIVATED NITINOL WITH DIMPLE RIGHT FORM (10)
Ortho Arch Company Inc
226-508
In Commercial Distribution

  • D9092265081 ()
226-508

  • Orthodontic archwire
.016 LOWER HEAT ACTIVATED NITINOL WITH DIMPLE RIGHT FORM (10)
Ortho Arch Company Inc
226-505
In Commercial Distribution

  • D90922650517 ()
226-505

  • Orthodontic archwire
.016 UPPER HEAT ACTIVATED NITINOL WITH DIMPLE RIGHT FORM (10)
Ortho Arch Company Inc
226-504
In Commercial Distribution

  • D90922650416 ()
226-504

  • Orthodontic archwire
.014 LOWER HEAT ACTIVATED NITINOL WITH DIMPLE RIGHT FORM (10)
Ortho Arch Company Inc
226-503
In Commercial Distribution

  • D90922650315 ()
226-503

  • Orthodontic archwire
.012 LOWER HEAT ACTIVATED NITINOL WITH DIMPLE RIGHT FORM (10)
Ortho Arch Company Inc
226-501
In Commercial Distribution

  • D90922650113 ()
226-501

  • Orthodontic archwire
.019 X .025 PRE-STOPPED HA COPPER NITI DAMON FORM (10)
Ortho Arch Company Inc
226-458
In Commercial Distribution

  • D9092264581 ()
226-458

  • Orthodontic archwire
.016 X .025 PRE-STOPPED HA COPPER NITI DAMON FORM (10)
Ortho Arch Company Inc
226-456
In Commercial Distribution

  • D9092264561 ()
226-456

  • Orthodontic archwire
.021 X .025 UPPER HEAT ACTIVATED NITINOL GLOBAL FORM (10)
Ortho Arch Company Inc
226-422G
In Commercial Distribution

  • D909226422G1 ()
226-422G

  • Orthodontic archwire
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