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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 34 of 34| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| DynaFORCE™ HiMax | 7115-1818 | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.0 mm Ti Cortex Screw Length 16 mm, Gold | FDA UDI | Class II | Active |
| DynaFORCE | DynaForce 10x10x10mm MotoClip Max C Implant Kit | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.5 mm Ti Variable Angle Screw Length 12 mm, Dark Purple | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.0 mm Ti Cortex Screw Length 24 mm, Rose Red | FDA UDI | Class II | Active |
| HiMAX Plus Implant System | HiMAX Plus Single Packaged Implant, 25mm x 22mm x 22mm | FDA UDI | Class II | Active |
| DynaFORCE Staple Instruments | DYNAFORCE MTP CONE REAMER, 24MM | FDA UDI | Class I | Active |
| CrossRoads 2.2mm Reamer | 1400-0022 | FDA UDI | Class II | Unknown |
| TriLeap Lower Extremity Anatomic Plating System | 2nd & 3rd Ti Lisfranc Joint Fusion Plate, Small, Left | FDA UDI | Class II | Active |
| Pro-Spec | COTTON OSTEOTOMY TRIAL 20MMX4.5MM | FDA UDI | Class I | Active |
| DynaFORCE Staple Instruments | DYNAFORCE, STANDARD INSERTER 25MM | FDA UDI | Class II | Active |
| DynaFORCE™ HiMax | DynaFORCE HiMAX Single Packaged Implant 20mm x 18mm x 14mm | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | Cuboid W Ti Plate, Standard | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.0 mm Ti Cortex Screw Length 60 mm, Rose Red | FDA UDI | Class II | Active |
| MotoBAND™ CP DynaForce® | DynaBunion Plate 15mm Right Single Pack | FDA UDI | Class II | Active |
| MOTOBAND Instruments | VIRTUGUIDE 0 RAC ROTATION - 10° - RT | FDA UDI | Class I | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| DynaFORCE™ | 3.2mm Staple Reamer | FDA UDI | Class II | Active |
| MOTOBAND Instruments | VIRTUGUIDE JOINT REAMING WIRE GUIDE | FDA UDI | Class I | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.0 mm Ti Cortex Screw Length 10 mm, Gold | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 2.5 mm Ti Cortex Screw Length 13 mm, Magenta | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | Bending Pin for 2.0 Plates | FDA UDI | Class I | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.5 mm Ti Cortex Screw Length 10 mm, Dark Purple | FDA UDI | Class II | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Active |
| MOTOBAND Instruments | LC LAPIDUS PLATE TEMPLATE- ALPHA | FDA UDI | Class I | Active |
| CrossRoads™ 3.5mm x 46mm Anti-Drift Bolt | 15LP-3546 | FDA UDI | Class II | Active |
| DynaForce MotoBAND Max | 7100-4H15 | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.0 mm Ti Variable Angle Screw Length 34 mm, Rose Red | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 2.5 mm Ti Cortex Screw Length 12 mm, Magenta | FDA UDI | Class II | Active |
| MIS Bunion Plating System | K190658 | FDA 510(k) | Class II | Active |
| CrossRoads Modular Tray System | K241050 | FDA 510(k) | Class II | Active |
| MotoBand(TM) CP Implant System | K160300 | FDA 510(k) | Class II | Active |
| MotoBand¿ CP Implant System | K152306 | FDA 510(k) | Class II | Active |
| MIS Bunion System | K181872 | FDA 510(k) | Class II | Active |
| CrossRoads Tray System | K202268 | FDA 510(k) | Class II | Active |
| MotoBAND CP Implant System | K173710 | FDA 510(k) | Class II | Active |
| STROPP (Single Tunnel Repair of Plantar Plate) | K160118 | FDA 510(k) | Class II | Active |
| MotoCLIP/HiMAX Implant System | K181410 | FDA 510(k) | Class II | Active |
| CrossRoads Screw System | K152072 | FDA 510(k)FDA UDI | Class II | Active |
| MotoBAND™ CP Implant System: DynaBunion™ 4D Minimal-incision Bunion System, DynaMET™ Lesser TMT Fusion System | K223342 | FDA 510(k) | Class II | Active |
| TRILEAP Plating System | K253178 | FDA 510(k) | Class II | Active |
| CrossTIE Intraosseous Fixation System | K151270 | FDA 510(k) | Class II | Active |
| MotoCLIP/HiMAX Step Staple Implant System | K181866 | FDA 510(k) | Class II | Active |
| FootHold System | K220797 | FDA 510(k) | Class II | Active |
| TriLEAP Plating System | K230591 | FDA 510(k) | Class II | Active |
Related Companies
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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. |