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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22mm, OsteoFlap
OSTEOMED LLC
219-0022
In Commercial Distribution

  • 00845694089456 ()

  • Outer Diameter: 22 Millimeter
219-0022

  • Craniofacial fixation plate kit, non-bioabsorbable
17mm, OsteoFlap
OSTEOMED LLC
219-0017
In Commercial Distribution

  • 00845694089449 ()

  • Outer Diameter: 17 Millimeter
219-0017

  • Craniofacial fixation plate kit, non-bioabsorbable
11mm, OsteoFlap
OSTEOMED LLC
219-0011
In Commercial Distribution

  • 00845694089432 ()

  • Outer Diameter: 11 Millimeter
219-0011

  • Craniofacial fixation plate kit, non-bioabsorbable
3.5mm Screw Module
OSTEOMED LLC
320-2913
In Commercial Distribution

  • 00845694089074 ()
320-2913

  • Instrument tray, reusable
EXTREMILOCK POST ANKLE FUSION 3 HOLE PL
OSTEOMED LLC
336-8003-SP-02
In Commercial Distribution

  • 00845694089067 ()

  • Length of Plate
  • Length: 3.3 Inch
336-8003-SP-02

  • Orthopaedic fixation plate, non-bioabsorbable
EXTREMILOCK ANT ANKLE FUSION 5H RIGHT PL
OSTEOMED LLC
336-7205-SP-02
In Commercial Distribution

  • 00845694088985 ()

  • Length of Plate
  • Length: 4.8 Inch
336-7205-SP-02

  • Orthopaedic fixation plate, non-bioabsorbable
EXTREMILOCK ANT ANKLE FUSION 5H LEFT PL
OSTEOMED LLC
336-7105-SP-02
In Commercial Distribution

  • 00845694088923 ()

  • Length: 4.8 Inch
  • Length of Plate
336-7105-SP-02

  • Orthopaedic fixation plate, non-bioabsorbable
220-0462, Purple ID Tag, Angled Locking
OSTEOMED LLC
220-0643-88
In Commercial Distribution

  • 00845694088794 ()
220-0643-88

  • General internal orthopaedic fixation system implantation kit
220-0461, Purple ID Tag, Angled Locking
OSTEOMED LLC
220-0643-87
In Commercial Distribution

  • 00845694088787 ()
220-0643-87

  • General internal orthopaedic fixation system implantation kit
220-0460, Purple ID Tag, Angled Locking
OSTEOMED LLC
220-0643-86
In Commercial Distribution

  • 00845694088770 ()
220-0643-86

  • General internal orthopaedic fixation system implantation kit
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