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 Type Device Class Implantable

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SP Pro Full Shell, High, Large
Elite Orthopaedics, Inc.
T98826
In Commercial Distribution

  • 00816591014308 ()
T98826

  • Ankle/foot orthosis
SP Pro Full Shell, High, Medium
Elite Orthopaedics, Inc.
T98824
In Commercial Distribution

  • 00816591014292 ()
T98824

  • Ankle/foot orthosis
SP Pro Full Shell, High, Small
Elite Orthopaedics, Inc.
T98822
In Commercial Distribution

  • 00816591014285 ()
T98822

  • Ankle/foot orthosis
Pro-Select Lace Up Ankle Brace, XX-Large
Elite Orthopaedics, Inc.
88415
In Commercial Distribution

  • 00816591014254 ()
88415

  • Ankle/foot orthosis
Pro Select Full Shell Walker, High, X-Large
Elite Orthopaedics, Inc.
T98628
In Commercial Distribution

  • 00816591014247 ()
T98628

  • Ankle/foot orthosis
Pediatric Night Splint
Elite Orthopaedics, Inc.
T58100
In Commercial Distribution

  • 00816591014230 ()
T58100

  • Ankle/foot orthosis
Adjustable Hybrid Dorsal Night Splint, Small/Medium
Elite Orthopaedics, Inc.
T59322
In Commercial Distribution

  • 00816591014223 ()
T59322

  • Ankle/foot orthosis
Plantar Fasciitis Wrap, Large/X-Large
Elite Orthopaedics, Inc.
T59826
In Commercial Distribution

  • 00816591014193 ()
T59826

  • Ankle/foot orthosis
Plantar Fasciitis Wrap, Small/Medium
Elite Orthopaedics, Inc.
T59822
In Commercial Distribution

  • 00816591014179 ()
T59822

  • Ankle/foot orthosis
Swedish Ankle Foot Orthosis, Men Left
Elite Orthopaedics, Inc.
T55170-L
In Commercial Distribution

  • 00816591014162 ()
T55170-L

  • Ankle/foot orthosis
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