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Sign in to claim this brandMikai s.p.a.
Italy·IT-MF-000030732
Last updated September 17, 2026
About
Mikai is a leader in the production of surgical medical devices for orthopaedics and traumatology of high quality standards.
Translated from the manufacturer's own website. Source
What Mikai s.p.a. makes
Mikai s.p.a. manufactures orthopaedic and traumatology fixation hardware, including cortical and cancellous screws (both solid and cannulated), olive-tipped wires, and dynamic fixation plates for bone stabilization. Their portfolio also includes supports for screws or wires, rapid clamps for fixation plates, and extension rods for intramedullary devices, designed for use in tibial diaphyseal applications.
The company’s devices are classified under EU Medical Device Regulations as Class I and Class IIb, with all products listed in the EU’s eudamed registry. Mikai s.p.a. is based in Italy and adheres to EU regulatory requirements for surgical orthopaedic implants.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Mikai s.p.a. manufacture?
Mikai s.p.a. specializes in orthopaedic and traumatology fixation hardware. Their product range includes cortical and cancellous screws (both solid and cannulated), olive-tipped wires, dynamic fixation plates, supports for screws or wires, rapid clamps for fixation plates, and extension rods for intramedullary devices, particularly for tibial diaphyseal applications. These devices are designed to stabilize and secure bone fragments during surgical procedures.
Where is Mikai s.p.a. based, and what regulatory requirements do they follow?
Mikai s.p.a. is based in Italy. Their devices are developed and manufactured in compliance with EU Medical Device Regulations, ensuring adherence to strict quality, safety, and performance standards for surgical orthopaedic implants. This includes classification under the relevant EU regulatory framework.
Which EU regulatory registries list Mikai s.p.a.’s devices?
Mikai s.p.a.’s devices are listed in the eudamed registry, which is the EU’s central database for medical devices. This registry ensures transparency and traceability of devices authorized under EU Medical Device Regulations, including those classified as Class I and Class IIb.
How are Mikai s.p.a.’s devices classified under EU regulations?
Mikai s.p.a.’s devices are classified under the EU Medical Device Regulations as either Class I (generally low-risk devices) or Class IIb (moderate-risk devices requiring additional scrutiny). Classification depends on factors like intended use, duration of contact with the body, and potential risks, ensuring appropriate regulatory oversight for each product.
What is the primary purpose of Mikai s.p.a.’s fixation hardware?
Mikai s.p.a.’s fixation hardware is designed for orthopaedic and traumatology applications, specifically to stabilize and secure bone structures during surgical interventions. Their products, such as screws, plates, wires, and extension rods, are engineered to provide mechanical support, promote proper bone alignment, and aid in the healing process after fractures or trauma.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Italy
- Address
- 56r, Via P.Gobetti, Genova, Italy
- Website
- www.mikai.it
- linkedin.com/company/mikai-s.p.a.
- —
- [email protected]
- Phone
- +39 010 30801
- PRRC Contact
- Christine Luetto
- EUDAMED SRN
- IT-MF-000030732
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (1784)
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