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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
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- FDA FEI Number
- 3020584246
- DUNS Number
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Catalogue (1696)
Page 21 of 34| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| MotoBAND™ CP DynaForce® | Anti-Drift Bolt Reamer Kit Pack-Out | FDA UDI | Class I | Active |
| Motoband Cp | 22.5° IM - 40° FP Right- 3D Correction Pin Guide | FDA UDI | Class I | Active |
| TriLeap Lower Extremity Anatomic Plating System | 2.0 mm Ti Cortex Screw Length 15 mm, Blue | FDA UDI | Class II | Active |
| DynaFORCE™ MotoCLIP Max | 7010-1010 | FDA UDI | N/A | Active |
| Motoband Cp | 10° IM - 0° FP Right- 3D Correction Pin Guide | FDA UDI | Class I | Active |
| TriLeap Lower Extremity Anatomic Plating System | Lapidus Ti Plate, Medial, Long | FDA UDI | Class II | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Active |
| Motoband Cp | 25° IM - 40° FP Left- 3D Correction Pin Guide | FDA UDI | Class I | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.0 mm Ti Variable Angle Screw Length 8 mm, Gold | FDA UDI | Class II | Active |
| Motoband Cp | 7.5° IM - 35° FP Right- 3D Correction Pin Guide | FDA UDI | Class I | Active |
| Motoband Cp | 25° IM - 5° FP Left - 3D Correction Pin Guide | FDA UDI | Class I | Active |
| MotoBAND | H10 Self Retaining Driver | FDA UDI | Class II | Active |
| DynaBunion | 1500-4801 | FDA UDI | Class I | Active |
| MotoBand | General Staple Plate Sharps Kit | FDA UDI | Class I | Active |
| Motoband Cp | 17.5° IM - 40° FP Right- 3D Correction Pin Guide | FDA UDI | Class I | Active |
| MotoBAND | MotoBAND CP, Non-Locking Screw, 3mm x 12mm - Sterile | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.0 mm Ti Variable Angle Screw Length 28 mm, Gold | FDA UDI | Class II | Active |
| Speedbutton | SpeedButton Kit 1x4mm | FDA UDI | Class II | Active |
| CrossRoads Screw System | 6.5mm x 110mm Support Beam Implant & Instrument Kit | FDA UDI | Class II | Active |
| Motoband Cp | 10° IM - 25° FP Right- 3D Correction Pin Guide | FDA UDI | Class I | Active |
| MotoBAND | MotoBAND CP, Non-Locking Screw, 3.5mm x 44mm - Sterile | FDA UDI | Class II | Active |
| MotoBAND CP | Midfoot Staple Plate - TMT Cuneiform Left 15mm Medium | FDA UDI | Class II | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| TriLeap Lower Extremity Anatomic Plating System | 2.0 Y-Shape Ti Fracture Plate, 6 Hole | FDA UDI | Class II | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| Motoband Cp | 12.5° IM - 10° FP Right - 3D Correction Pin Guide | FDA UDI | Class I | Active |
| Motoband Cp | 25° IM - 15° FP Right- 3D Correction Pin Guide | FDA UDI | Class I | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Active |
| Motoband Cp | 7.5° IM - 45° FP Right- 3D Correction Pin Guide | FDA UDI | Class I | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.0 mm Ti Cortex Screw Length 10 mm, Rose Red | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | Screw Rack for 3.0/3.5/4.0 Screws | FDA UDI | Class II | 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 | 3.5 mm Ti Variable Angle Screw Length 50 mm, Dark Purple | FDA UDI | Class II | Active |
| CrossRoads™ Screw | Headless | FDA UDI | Class II | Active |
| MotoBAND | MotoBAND CP, Polyaxial Locking Screw, 3mm x 14mm - Sterile | FDA UDI | Class II | Active |
| MotoBAND | MotoBAND CP, Locking Screw, 3mm x 18mm - Sterile | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | NC Ti Fusion 5 hole, Long, Left | FDA UDI | Class II | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Active |
| MOTOBAND Instruments | MOTOBAND CP LARGE PLATE BENDER | FDA UDI | Class I | Active |
| TriLeap Lower Extremity Anatomic Plating System | 2nd & 3rd Ti Lisfranc Joint Fusion Plate, Large, Left | FDA UDI | Class II | Active |
| Motoband Cp | 30° IM - 30° FP Right- 3D Correction Pin Guide | FDA UDI | Class I | Active |
| CrossRoads™ Screw | Headless | FDA UDI | Class II | Active |
| CrossRoads™ Screw | Headless | FDA UDI | Class II | Active |
| HiMAX Plus Implant System | HiMAX Plus Single Packaged Implant, 15mm x 15mm x 15mm | FDA UDI | Class II | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Active |
| MotoBAND | Implant, MotoBAND CP, MTP Plate, Right - Sterile | FDA UDI | Class II | Active |
| MotoBAND | Implant, 3.5mm x 42mm Anti-Drift Bolt, Fully Threaded | FDA UDI | Class II | Active |
| Pro-Spec | MTP TRIAL 18MM x 20MM | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
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.
| 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. |