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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 32 of 34| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| MOTOBAND Instruments | 18MM Z TEMPLATE | FDA UDI | Class I | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| TriLeap Lower Extremity Anatomic Plating System | 3.5 mm Ti Variable Angle Screw Length 14 mm, Dark Purple | FDA UDI | Class II | Active |
| MotoBAND™ CP DynaForce® MPJ | 7R50-1018 | FDA UDI | Class II | Unknown |
| CrossRoads™ Bone Screw | Snap-Off Screw Driver - One Piece | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 4.0 mm Ti Variable Angle Screw Length 56 mm, Green | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | Navicular Ti Plate, Short | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 4.0 mm Ti Cortex Screw Length 28 mm, Green | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 1st MTP Ti Fusion Plate, Small, 10 Deg, Left | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 1st MTP Ti Fusion Revision Plate, Medium, 5 Deg, Right | FDA UDI | Class II | Active |
| CrossRoads™ Bone Screw | Headless | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | Navicular Ti Plate, Long | FDA UDI | Class II | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| HiMAX Plus Implant System | HiMAX Plus Single Packaged Implant, 18mm x 18mm x 18mm | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 2nd & 3rd Ti Lisfranc Joint Fusion Plate, Medium, Left | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.0 mm Ti Variable Angle Screw Length 13 mm, Gold | FDA UDI | Class II | Active |
| DynaFORCE™ | 7010-1010KT | FDA UDI | N/A | Active |
| MotoBAND™ CP DynaForce® MPJ | 7R50-0018 | FDA UDI | Class II | Unknown |
| TriLeap Lower Extremity Anatomic Plating System | 3.0 mm Ti Variable Angle Screw Length 26 mm, Gold | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 2.0 mm Ti Variable Angle Screw Length 26 mm, Blue | FDA UDI | Class II | Active |
| MiniBunion™ | MiniBunion, Non-Locking Screw, 2.7mm x 18mm - Sterile | FDA UDI | Class II | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 4.0 mm Ti Cortex Screw Length 20 mm, Green | FDA UDI | Class II | Active |
| MotoBAND CP DynaFORCE™ | Universal Handle | FDA UDI | Class I | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Active |
| MotoBAND CP DynaFORCE™ | Compressor Block | FDA UDI | Class I | Active |
| MOTOBAND Instruments | VIRTUGUIDE 0 RAC ROTATION - 10° - LT | FDA UDI | Class I | Active |
| TriLeap Lower Extremity Anatomic Plating System | 4.0 mm Ti Variable Angle Screw Length 24 mm, Green | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 4.0 mm Ti Cortex Screw Length 48 mm, Green | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 4.0 mm Ti Variable Angle Screw Length 58 mm, Green | FDA UDI | Class II | Active |
| DynaFORCE™ HiMax | DynaFORCE HiMAX Single Packaged Implant 25mm x 18mm x 18mm | FDA UDI | Class II | Active |
| DynaForce MotoBAND Max | 7100-RP15 | FDA UDI | Class II | Unknown |
| Pro-Spec | EVANS OSTEOTOMY TRIAL 22MMX8MM | FDA UDI | Class I | Active |
| TriLeap Lower Extremity Anatomic Plating System | 2.0 mm Ti Cortex Screw Length 10 mm, Blue | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 2.0 mm Ti Variable Angle Screw Length 9 mm, Blue | FDA UDI | Class II | Active |
| HiMAX Plus Implant System | HiMAX Plus Single Packaged Implant, 18mm x 18mm x 14mm | FDA UDI | Class II | Active |
| CrossRoads™ Bone Screw | Headed | FDA UDI | Class II | Unknown |
| DynaForce MotoBAND Max | 7100-ZA15 | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 24MM Cannulated Cup Reamer | FDA UDI | Class I | Active |
| Pro-Spec | LAPIDUS TRIAL 8MM | FDA UDI | Class I | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.0 mm Ti Variable Angle Screw Length 11 mm, Gold | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.0 mm Ti Cortex Screw Length 40 mm, Rose Red | FDA UDI | Class II | Active |
| TriLeap Lower Extremity Anatomic Plating System | 2.5 mm Ti Cortex Screw Length 20 mm, Magenta | FDA UDI | Class II | Active |
| MiniBunion™ | MiniBunion, Polyaxial Locking Screw, 3mm x 20mm - Sterile | FDA UDI | Class II | Active |
| MOTOBAND Instruments | CORA JOYSTICK | FDA UDI | Class I | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.5 mm Ti Cortex Screw Length 50 mm, Dark Purple | FDA UDI | Class II | Active |
| DynaFORCE™ HiMax | DynaFORCE HiMAX Single Packaged Implant 25mm x 18mm x 14mm | FDA UDI | Class II | Active |
| DynaFORCE™ | 7015-1212KT | FDA UDI | N/A | Active |
| TriLeap Lower Extremity Anatomic Plating System | 3.0 mm Ti Cortex Screw Length 40 mm, Gold | FDA UDI | Class II | Active |
| Pro-Spec | LAPIDUS TRIAL 10MM | 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. |