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Sign in to claim this brandCitieffe
US
Last updated May 23, 2026
What Citieffe makes
Citieffe manufactures orthopaedic bone screws, femur and tibia intramedullary nails, external fixation systems, medullary canal reamers, trocar blades, surgical drill bits, and implant aiming or guiding blocks. These devices are primarily reusable or single-use sterile instruments and implants used in orthopaedic surgery.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA's Global Unique Device Identification Database (GUDID). Citieffe is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of devices does Citieffe manufacture?
Citieffe manufactures orthopaedic bone screws, femur and tibia intramedullary nails, external fixation systems, medullary canal reamers, trocar blades, surgical drill bits, and implant aiming or guiding blocks. These are primarily reusable or single-use sterile instruments and implants used in orthopaedic surgery, as stated in the device data summary.
Where is Citieffe based?
Citieffe is based in the United States, as explicitly stated in the SUMMARY section of the device data, which confirms the company's country of origin as US.
Which regulatory registries list Citieffe's devices?
Citieffe's devices are listed in the FDA's Global Unique Device Identification Database (GUDID), as indicated by the LISTED IN field showing 'fda_udi', which refers to the FDA UDI system and its public GUDID repository.
How are Citieffe's devices classified?
Citieffe's devices are classified as Class I and Class II medical devices, according to the DEVICE CLASSES field in the device data, which specifies these two classification levels without assigning any to specific products.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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- EUDAMED SRN
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Catalogue (1464)
Page 30 of 30| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Eba2 | Long nail ø10mm L460mm, left | FDA UDI | Class II | Active |
| Rondo' | Screw ø7.5mm L40-35mm | FDA UDI | Class II | Active |
| Dolphix | Soft tissue protection guide | FDA UDI | Class II | Unknown |
| Orthopaedic Surgical Instruments | Reamers tray | FDA UDI | Class I | Active |
| Rondo' | Rondo' cannulated screw ø8mm L60mm | FDA UDI | Class II | Active |
| Dolphix | SS Bone screw ø6mm L200-45mm, Low Reflex | FDA UDI | Class II | Active |
| Eba2 | Standard and medium nail guide | FDA UDI | Class II | Active |
| Orthopaedic Surgical Instruments | Cannula with handle ø16mm | FDA UDI | Class I | Active |
| Rondo' | Screw ø8mm L60-20mm | FDA UDI | Class II | Active |
| Eba2 | Cephalic screw ø7.5mm L85mm | FDA UDI | Class II | Active |
| Rondo' | Rondo' cannulated screw ø8mm L95mm | FDA UDI | Class II | Active |
| Citieffe Titanium Nailing System | K113387 | FDA 510(k) | Class II | Active |
| Citieffe-Titanium Cannulated Screw | K113388 | FDA 510(k) | Class II | Active |
| External Fixator St.a R 90 F4 | K113384 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Citieffe Srl Calderara di Reno Bologna · IT FEI 3003249380