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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.019 X .025 HA NITINOL WITH COPPER DAMON FORM (10)
Ortho Arch Company Inc
.019 X .025 DAMON FORM
In Commercial Distribution

  • D909226420CD1 ()
226-420CD

  • Orthodontic archwire
.019 X .025 UPPER HEAT ACTIVATED NITINOL WITH COPPER (10)
Ortho Arch Company Inc
226-420C
In Commercial Distribution

  • D909226420C1 ()
226-420C

  • Orthodontic archwire
.019 X .025 UPPER HEAT ACTIVATED NITINOL RIGHT FORM (10)
Ortho Arch Company Inc
226-420
In Commercial Distribution

  • D90922642013 ()
226-420

  • Orthodontic archwire
.018 X .025 LOWER HEAT ACTIVATED NITINOL GLOBAL FORM (10)
Ortho Arch Company Inc
226-419G
In Commercial Distribution

  • D909226419G1 ()
226-419G

  • Orthodontic archwire
.018 X .025 LOWER HEAT ACTIVATED NITINOL WITH COPPER (10)
Ortho Arch Company Inc
226-419C
In Commercial Distribution

  • D909226419C1 ()
226-419C

  • Orthodontic archwire
.018 X .025 LOWER HEAT ACTIVATED NITINOL RIGHT FORM (10)
Ortho Arch Company Inc
226-419
In Commercial Distribution

  • D9092264191 ()
226-419

  • Orthodontic archwire
.018 X .025 UPPER HEAT ACTIVATED NITINOL GLOBAL FORM (10)
Ortho Arch Company Inc
226-418G
In Commercial Distribution

  • D909226418G1 ()
226-418G

  • Orthodontic archwire
.018 X .025 UPPER HEAT ACTIVATED NITINOL WITH COPPER (10)
Ortho Arch Company Inc
226-418C
In Commercial Distribution

  • D909226418C1 ()
226-418C

  • Orthodontic archwire
.018 X .025 UPPER HEAT ACTIVATED NITINOL RIGHT FORM (10)
Ortho Arch Company Inc
226-418
In Commercial Distribution

  • D9092264181 ()
226-418

  • Orthodontic archwire
.018 X .018 LOWER HEAT ACTIVATED NITINOL GLOBAL FORM (10)
Ortho Arch Company Inc
226-417G
In Commercial Distribution

  • D909226417G1 ()
226-417G

  • Orthodontic archwire
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