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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
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Facebook
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Email
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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 3 of 34
DeviceModel / ReferenceRegistriesClassStatus
TriLeap Lower Extremity Anatomic Plating System Depth Gauge for 3.0/3.5/4.0 Screws
FDA UDI
Class IActive
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIActive
Motoband Cp 12.5° IM - 35° FP Right- 3D Correction Pin Guide
FDA UDI
Class IActive
Motoband Cp 25° IM - 15° FP Left - 3D Correction Pin Guide
FDA UDI
Class IActive
MotoBAND DynaForce MTP Standard Plate with Slot, 5deg valgus, 0deg dorsiflexion, 18mm Cli
FDA UDI
Class IIActive
Motoband Cp 7.5° IM - 30° FP Right- 3D Correction Pin Guide
FDA UDI
Class IActive
Motoband Cp 30° IM - 10° FP Right- 3D Correction Pin Guide
FDA UDI
Class IActive
MotoBAND CP 7100-UA5N
FDA UDI
Class IIActive
DynaForce MotoBAND Max 7100-ZB18
FDA UDI
Class IIActive
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIUnknown
TriLeap Lower Extremity Anatomic Plating System Bending Pin for 3.0/3.5/4.0 Plates
FDA UDI
Class IActive
TriLeap Lower Extremity Anatomic Plating System 2.5 mm Ti Cortex Screw Length 36 mm, Magenta
FDA UDI
Class IIActive
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIUnknown
MotoBAND DynaForce MTP Standard Plate with Slot, 5deg valgus, 5deg dorsiflexion, 18mm Cli
FDA UDI
Class IIActive
CrossTIE™ H10 Driver Cannulated 1456-0015
FDA UDI
Class IIActive
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIUnknown
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIActive
CrossRoads Screw System 6.5mm x 115mm Support Beam Implant & Instrument Kit
FDA UDI
Class IIActive
HiMAX Plus Implant System HiMAX Plus Single Packaged Implant, 18mm x 20mm x 20mm
FDA UDI
Class IIActive
TriLeap Lower Extremity Anatomic Plating System 14MM Cannulated Cup Reamer
FDA UDI
Class IActive
TriLeap Lower Extremity Anatomic Plating System 2.5 mm Ti Cortex Screw Length 11 mm, Magenta
FDA UDI
Class IIActive
HiMAX Plus Implant System HiMAX Plus Single Packaged Implant, 15mm x 18mm x 18mm
FDA UDI
Class IIActive
Motoband Cp 30° IM - 15° FP Left - 3D Correction Pin Guide
FDA UDI
Class IActive
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIUnknown
MotoBAND Implant, MotoBAND CP, Double Y Plate, Right
FDA UDI
Class IIActive
Pro-Spec SUB-TALAR TRIAL 14MM
FDA UDI
Class IActive
HiMAX C DynaFORCE HIMAX C Implant Kit, 20 x 20 x 20
FDA UDI
Class IIActive
MotoBAND MotoBAND CP, Polyaxial Locking Screw, 3mm x 26mm - Sterile
FDA UDI
Class IIActive
HiMAX C 7118-2222KT-C
FDA UDI
Class IIActive
Motoband Cp 15° IM - 45° FP Left- 3D Correction Pin Guide
FDA UDI
Class IActive
MotoBAND™ CP Lapidus LZ Beta 18mm
FDA UDI
Class IIActive
MOTOBAND Instruments CROSSROADS STAPLE TAMP
FDA UDI
Class IActive
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIUnknown
TriLeap Lower Extremity Anatomic Plating System 2.0 Straight Ti Fracture Plate, 5 Hole
FDA UDI
Class IIActive
TriLeap Lower Extremity Anatomic Plating System Compression Wire 1.6mm for 3.0/3.5/4.0 Plates, Thread Length 25mm
FDA UDI
Class IActive
MotoBAND™ CP DynaForce® DynaForce Reamer, 2.0mm Sterile Packaged
FDA UDI
Class IActive
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIUnknown
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIActive
Motoband Cp 22.5° IM - 5° FP Left - 3D Correction Pin Guide
FDA UDI
Class IActive
MotoBAND MotoBAND CP, Locking Screw, 3mm x 40mm - Sterile
FDA UDI
Class IIActive
TriLeap Lower Extremity Anatomic Plating System Cone Drill Guide for 2.0 Drill Bit, Magenta/Gold
FDA UDI
Class IActive
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIActive
TriLeap Lower Extremity Anatomic Plating System 16MM Cannulated Cone Reamer
FDA UDI
Class IActive
CrossTIE™ 1443-2500
FDA UDI
Class IIActive
Motoband Cp 25° IM - 0° FP Right- 3D Correction Pin Guide
FDA UDI
Class IActive
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIUnknown
CrossRoads™ Bone Screw Headed
FDA UDI
Class IIUnknown
TriLeap Lower Extremity Anatomic Plating System 1st MTP Ti Fusion Plate, Medium, 0 Deg, Right
FDA UDI
Class IIActive
Pro-Spec COTTON OSTEOTOMY TRIAL 16MMX5.5MM
FDA UDI
Class IActive
TriLeap Lower Extremity Anatomic Plating System 1st MTP Ti Fusion Revision Plate, Small, 0 Deg, Right
FDA UDI
Class IIActive

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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.