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CROSSROADS EXTREMITY SYSTEMS LLC

US

Last updated September 17, 2026

Information

Country
US
Address
6423 Shelby View Dr, Memphis, TN, 38134
Website
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LinkedIn
—
Facebook
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Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
3020584246
DUNS Number
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Catalogue (1696)

Page 24 of 34
DeviceModel / ReferenceRegistriesClassStatus
Motoband Cp 0 Rac 10°FP - Right
FDA UDI
Class IActive
Motoband Cp 17.5° IM - 25° FP Left - 3D Correction Pin Guide
FDA UDI
Class IActive
MotoBAND MotoBAND CP, Polyaxial Locking Screw, 3.5mm x 34mm - Sterile
FDA UDI
Class IIActive
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIUnknown
CrossRoads™ Screw Headless
FDA UDI
Class IIActive
MotoBAND CP Midfoot Staple Plate - L - Beta - 18mm
FDA UDI
Class IIActive
MotoBAND MotoBAND CP, Polyaxial Locking Screw, 3.5mm x 26mm - Sterile
FDA UDI
Class IIActive
MotoBAND MotoBAND CP, Locking Screw, 3.5mm x 12mm - Sterile
FDA UDI
Class IIActive
DynaBunion DynaBunion RACBlock, Size 2
FDA UDI
Class IActive
TriLeap Lower Extremity Anatomic Plating System 3.5 mm Ti Cortex Screw Length 32 mm, Dark Purple
FDA UDI
Class IIActive
Pro-Spec LAPIDUS TRIAL 12MM
FDA UDI
Class IActive
TriLeap Lower Extremity Anatomic Plating System 3.0 mm Ti Variable Angle Screw Length 28 mm, Rose Red
FDA UDI
Class IIActive
MotoBAND MotoBAND CP, Polyaxial Locking Screw, 3mm x 22mm - Sterile
FDA UDI
Class IIActive
DynaForce MotoBAND Max 7100-5H15
FDA UDI
Class IIActive
TriLeap Lower Extremity Anatomic Plating System Lapidus Screw Targeting Guide Right
FDA UDI
Class IActive
TriLeap Lower Extremity Anatomic Plating System 4.0 mm Ti Cortex Screw Length 32 mm, Green
FDA UDI
Class IIActive
CrossTIE™ Individual Implant
FDA UDI
Class IIActive
Motoband Cp 27.5° IM - 20° FP Left - 3D Correction Pin Guide
FDA UDI
Class IActive
TriLeap Lower Extremity Anatomic Plating System Cone Guide Inserter
FDA UDI
Class IActive
MotoBAND Implant, 3.5mm x 36mm Anti-Drift Bolt
FDA UDI
Class IIActive
Motoband Cp 17.5° IM - 10° FP Left- 3D Correction Pin Guide
FDA UDI
Class IActive
CrossRoads™ Bone Screw Snap-Off
FDA UDI
Class IIActive
MotoBAND MotoBAND CP, Non-Locking Screw, 3.5mm x 30mm - Sterile
FDA UDI
Class IIActive
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIUnknown
Pro-Spec SUB-TALAR TRIAL 10MM
FDA UDI
Class IActive
MOTOBAND Instruments VIRTUGUIDE 1 RAC ROTATION - 5° - LT
FDA UDI
Class IActive
MotoBAND CP DynaFORCE™ Wire Template
FDA UDI
Class IActive
CrossRoads™ Bone Screw Snap-Off
FDA UDI
Class IIActive
Motoband Cp 20° IM - 35° FP Right- 3D Correction Pin Guide
FDA UDI
Class IActive
TriLeap Lower Extremity Anatomic Plating System 4.0 mm Ti Cortex Screw Length 14 mm, Green
FDA UDI
Class IIActive
MotoBAND MotoBAND CP, Non-Locking Screw, 3.5mm x 26mm - Sterile
FDA UDI
Class IIActive
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIUnknown
MotoCLIP™ 1412-1212
FDA UDI
Class IIActive
MotoBAND™ CP DynaForce® MPJ 7L50-1018
FDA UDI
Class IIUnknown
TriLeap Lower Extremity Anatomic Plating System 3.0 mm Ti Cortex Screw Length 42 mm, Rose Red
FDA UDI
Class IIActive
Pro-Spec MTP TRIAL 20MM x 8MM
FDA UDI
Class IActive
Motoband Cp 22.5° IM - 5° FP Right- 3D Correction Pin Guide
FDA UDI
Class IActive
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIUnknown
HiMAX C 7118-1414-C
FDA UDI
Class IIActive
MotoBAND Implant, 3.5mm x 28mm Anti-Drift Bolt
FDA UDI
Class IIActive
MotoBAND CP 7100-UB5N
FDA UDI
Class IIActive
Motoband Cp 20° IM - 0° FP Right- 3D Correction Pin Guide
FDA UDI
Class IActive
MiniBunion MiniBunion Non-Locking Drill Guide
FDA UDI
Class IActive
MotoBAND CP DynaFORCE™ Compressor Block, Size 3
FDA UDI
Class IActive
MotoCLIP™ Single Pack Implant
FDA UDI
Class IIActive
MotoBAND CP DynaFORCE™ K-wires, 1.6mm
FDA UDI
Class IActive
MotoBAND CP Midfoot Staple Plate - U - Alpha-18mm
FDA UDI
Class IIActive
MotoBAND MotoBAND CP, Non-Locking Screw, 3.5mm x 42mm - Sterile
FDA UDI
Class IIActive
TriLeap Lower Extremity Anatomic Plating System 3.0 mm Ti Cortex Screw Length 15 mm, Gold
FDA UDI
Class IIActive
MotoCLIP™ 1418-1818
FDA UDI
N/AActive

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Importers

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Notified Bodies

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Authorities

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FDA Recalls (2)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Sep 19, 2019Z-0212-2020—terminated

Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.

Feb 16, 2017Z-1487-2017—terminated

Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and labeled as 18mm x 14mm x 14mm.