Citieffe
Country not established FDA
- Devices
- 1,579
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
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.
Catalogue
Search and filter all 1,579 devicesShowing 1-50 of 1,579
FDA establishments
- Citieffe SRL Calderara di Reno Bologna · IT FEI 3003249380
Frequently asked questions
How many devices does Citieffe have in the registry?
The registry currently lists 1579 devices for Citieffe. Devices recorded under merged duplicate company entries are counted once.
Which registries list Citieffe's devices?
Among its 50 most recently registered devices, Citieffe has devices listed in EUDAMED (4 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Citieffe's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Citieffe's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Citieffe in the registry?
The most recently registered devices listed for Citieffe include Orthopaedic Surgical Instruments Cephalic drill with notches, ST.A.R. 90 F4 Pin and rod clamp kit, Orthopaedic Surgical Instruments Drill bit, ø3.5x195mm and ST.A.R. 90 F4 Knee fixator distractor.
Which FDA establishments are linked to Citieffe?
1 FDA establishment is linked to Citieffe in the registry; they are listed on the company page.