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CROSSROADS EXTREMITY SYSTEMS LLC

Last updated September 17, 2026

Information

Country: US
Address: 6423 Shelby View Dr, Memphis, TN, 38134
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EUDAMED SRN: —
FDA FEI Number: 3020584246
DUNS Number: —

Catalogue (1696)

Page 9 of 34

Device	Model / Reference	Registries	Class	Status
MotoBAND™ CP DynaForce® MPJ	MPJ Short 5deg Valgus/10deg Dorsiflexion	FDA UDI	Class II	Active
Motoband Cp	22.5° IM - 0° FP Right- 3D Correction Pin Guide	FDA UDI	Class I	Active
MotoBAND CP DynaFORCE™	Temporary Fixation Pins 2.2mm	FDA UDI	Class I	Active
CrossRoads™ Bone Screw	Headed	FDA UDI	Class II	Active
DyanBunion	DynaBunion Plate SHORT 15mm - LEFT	FDA UDI	Class II	Active
MotoBAND	MotoBAND CP, Locking Screw, 3mm x 26mm - Sterile	FDA UDI	Class II	Active
CrossRoads Modular Tray System	CROSSROADS KEEL-LOCK CADDY	FDA UDI	Class II	Active
Motoband Cp	17.5° IM - 40° FP Left- 3D Correction Pin Guide	FDA UDI	Class I	Active
MotoBAND CP	Midfoot Staple Plate - TMT Cuneiform Left 15mm Large	FDA UDI	Class II	Active
Pro-Spec	MTP TRIAL 20MM x 10MM	FDA UDI	Class I	Active
DynaFORCE Staple Instruments	MOTOCLIP INSERTER ASSEMBLY, 10X10	FDA UDI	Class II	Active
MotoCLIP/HiMAX Step Staple	Single Pack, 18mm x 22mm x 24mm, 6mm Offset	FDA UDI	Class II	Active
MotoCLIP™	1418-2020	FDA UDI	N/A	Active
TriLeap Lower Extremity Anatomic Plating System	2.5 mm Ti Variable Angle Screw Length 28 mm, Magenta	FDA UDI	Class II	Active
MotoBAND	Implant, MotoBAND CP, 5-Hole Straight Plate - Sterile	FDA UDI	Class II	Active
Motoband Cp	10° IM - 10° FP Right - 3D Correction Pin Guide	FDA UDI	Class I	Active
DynaFORCE Vero Plate Trial Kit - Proximal	7000-RPTK-P	FDA UDI	Class I	Active
MotoBAND	MotoBAND CP, Polyaxial Locking Screw, 3mm x 12mm - Sterile	FDA UDI	Class II	Active
MOTOBAND Instruments	OBLIQUE K-WIRE GUIDE	FDA UDI	Class I	Active
TriLeap Lower Extremity Anatomic Plating System	1st & 2nd Ti Lisfranc Joint Fusion Plate, Medium, Left	FDA UDI	Class II	Active
Motoband Cp	22.5° IM - 45° FP Left- 3D Correction Pin Guide	FDA UDI	Class I	Active
DynaFORCE Staple Instruments	DYNAFORCE, DRILL GUIDE, 25MM	FDA UDI	Class I	Active
DynaBunion	DynaBunion RAC Block, Size 0	FDA UDI	Class I	Active
Motoband Cp	12.5° IM - 30° FP Left - 3D Correction Pin Guide	FDA UDI	Class I	Active
DynaForce MotoBAND Max	7100-ZA18	FDA UDI	Class II	Active
Motoband Cp	12.5° IM - 45° FP Left- 3D Correction Pin Guide	FDA UDI	Class I	Active
Motoband Cp	12.5° IM - 45° FP Right- 3D Correction Pin Guide	FDA UDI	Class I	Active
CrossRoads™ Bone Screw	Headed	FDA UDI	Class II	Active
MotoBAND	MotoBAND CP, Locking Screw, 3mm x 30mm - Sterile	FDA UDI	Class II	Active
DynaFORCE Staple Instruments	DYNAFORCE MTP CUP REAMER, 20MM	FDA UDI	Class I	Active
CrossRoads Screw System	3.0 Headed Implant Prep Kit Including Reamer	FDA UDI	Class I	Active
MotoCLIP™	1442-1814	FDA UDI	N/A	Active
Pro-Spec	EVANS OSTEOTOMY TRIAL 18MMX12MM	FDA UDI	Class I	Active
CrossRoads™ Bone Screw	Snap-Off	FDA UDI	Class II	Active
TriLeap Lower Extremity Anatomic Plating System	Implant Module for MTP Fusion Plates	FDA UDI	Class II	Active
Motoband Cp	22.5° IM - 15° FP Right- 3D Correction Pin Guide	FDA UDI	Class I	Active
MotoBAND CP Non Locking Drill Guide	130505	FDA UDI	Class I	Unknown
CrossRoads™ Screw	7.0 Headless Implant Prep Kit	FDA UDI	Class I	Active
CrossRoads™ Bone Screw	Headed	FDA UDI	Class II	Unknown
MotoCLIP™	1418-1822	FDA UDI	N/A	Active
MotoBAND	MotoBAND CP, Locking Screw, 3mm x 14mm	FDA UDI	Class II	Active
MotoBAND	MotoBAND CP 2.0mm Reamer - Sterile	FDA UDI	Class II	Unknown
DynaBunion	DynaBunion Plate STD 15mm - Right	FDA UDI	Class II	Active
DynaForce MotoBAND Max	7100-TJ18	FDA UDI	Class II	Active
CrossRoads™ Bone Screw	Headed	FDA UDI	Class II	Unknown
CrossRoads™ Bone Screw	Headed	FDA UDI	Class II	Unknown
CrossRoads™ Bone Screw	Headed	FDA UDI	Class II	Unknown
TriLeap Lower Extremity Anatomic Plating System	Coaxial Drill Guide for 2.0 Drill Bit, Magenta/Gold	FDA UDI	Class I	Active
Motoband Cp	25° IM - 35° FP Left- 3D Correction Pin Guide	FDA UDI	Class I	Active
DynaFORCE Staple Instruments	DYNAFORCE, DRILL GUIDE, 20MM	FDA UDI	Class I	Active

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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.

Date	Recall No.	Class	Status	Reason
Sep 19, 2019	Z-0212-2020	—	terminated	Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.
Feb 16, 2017	Z-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.