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Sign in to claim this brandCROSSROADS 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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- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3020584246
- DUNS Number
- —
Catalogue (1696)
Page 3 of 34| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| TriLeap Lower Extremity Anatomic Plating System | Depth Gauge for 3.0/3.5/4.0 Screws | FDA UDI | Class I | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Active |
| Motoband Cp | 12.5° IM - 35° FP Right- 3D Correction Pin Guide | FDA UDI | Class I | Active |
| Motoband Cp | 25° IM - 15° FP Left - 3D Correction Pin Guide | FDA UDI | Class I | Active |
| MotoBAND | DynaForce MTP Standard Plate with Slot, 5deg valgus, 0deg dorsiflexion, 18mm Cli | FDA UDI | Class II | Active |
| Motoband Cp | 7.5° IM - 30° FP Right- 3D Correction Pin Guide | FDA UDI | Class I | Active |
| Motoband Cp | 30° IM - 10° FP Right- 3D Correction Pin Guide | FDA UDI | Class I | Active |
| MotoBAND CP | 7100-UA5N | FDA UDI | Class II | Active |
| DynaForce MotoBAND Max | 7100-ZB18 | FDA UDI | Class II | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| TriLeap Lower Extremity Anatomic Plating System | Bending Pin for 3.0/3.5/4.0 Plates | FDA UDI | Class I | Active |
| TriLeap Lower Extremity Anatomic Plating System | 2.5 mm Ti Cortex Screw Length 36 mm, Magenta | FDA UDI | Class II | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| MotoBAND | DynaForce MTP Standard Plate with Slot, 5deg valgus, 5deg dorsiflexion, 18mm Cli | FDA UDI | Class II | Active |
| CrossTIE™ H10 Driver Cannulated | 1456-0015 | FDA UDI | Class II | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Active |
| CrossRoads Screw System | 6.5mm x 115mm Support Beam Implant & Instrument Kit | FDA UDI | Class II | Active |
| HiMAX Plus Implant System | HiMAX Plus Single Packaged Implant, 18mm x 20mm x 20mm | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 14MM Cannulated Cup Reamer | FDA UDI | Class I | Active |
| TriLeap Lower Extremity Anatomic Plating System | 2.5 mm Ti Cortex Screw Length 11 mm, Magenta | FDA UDI | Class II | Active |
| HiMAX Plus Implant System | HiMAX Plus Single Packaged Implant, 15mm x 18mm x 18mm | FDA UDI | Class II | Active |
| Motoband Cp | 30° IM - 15° FP Left - 3D Correction Pin Guide | FDA UDI | Class I | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| MotoBAND | Implant, MotoBAND CP, Double Y Plate, Right | FDA UDI | Class II | Active |
| Pro-Spec | SUB-TALAR TRIAL 14MM | FDA UDI | Class I | Active |
| HiMAX C | DynaFORCE HIMAX C Implant Kit, 20 x 20 x 20 | FDA UDI | Class II | Active |
| MotoBAND | MotoBAND CP, Polyaxial Locking Screw, 3mm x 26mm - Sterile | FDA UDI | Class II | Active |
| HiMAX C | 7118-2222KT-C | FDA UDI | Class II | Active |
| Motoband Cp | 15° IM - 45° FP Left- 3D Correction Pin Guide | FDA UDI | Class I | Active |
| MotoBAND™ CP Lapidus | LZ Beta 18mm | FDA UDI | Class II | Active |
| MOTOBAND Instruments | CROSSROADS STAPLE TAMP | FDA UDI | Class I | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| TriLeap Lower Extremity Anatomic Plating System | 2.0 Straight Ti Fracture Plate, 5 Hole | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | Compression Wire 1.6mm for 3.0/3.5/4.0 Plates, Thread Length 25mm | FDA UDI | Class I | Active |
| MotoBAND™ CP DynaForce® | DynaForce Reamer, 2.0mm Sterile Packaged | FDA UDI | Class I | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Active |
| Motoband Cp | 22.5° IM - 5° FP Left - 3D Correction Pin Guide | FDA UDI | Class I | Active |
| MotoBAND | MotoBAND CP, Locking Screw, 3mm x 40mm - Sterile | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | Cone Drill Guide for 2.0 Drill Bit, Magenta/Gold | FDA UDI | Class I | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 16MM Cannulated Cone Reamer | FDA UDI | Class I | Active |
| CrossTIE™ | 1443-2500 | FDA UDI | Class II | Active |
| Motoband Cp | 25° IM - 0° FP Right- 3D Correction Pin Guide | FDA UDI | Class I | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| TriLeap Lower Extremity Anatomic Plating System | 1st MTP Ti Fusion Plate, Medium, 0 Deg, Right | FDA UDI | Class II | Active |
| Pro-Spec | COTTON OSTEOTOMY TRIAL 16MMX5.5MM | FDA UDI | Class I | Active |
| TriLeap Lower Extremity Anatomic Plating System | 1st MTP Ti Fusion Revision Plate, Small, 0 Deg, Right | FDA UDI | Class II | Active |
Related Companies
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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. |