Made in Italy medical devices for extremity surgery, born from surgical experience, built to last.
Made in Italy medical devices for extremity surgery, born from surgical experience, built to last.
BRM Extremities is an Italian company specializing in the design and production of orthopedic medical devices for the extremities. We operate in a context of continuous technological innovation, developing solutions in close collaboration with Italian and international specialist surgeons.
OBJECTIVE
To create devices that meet the real needs of surgeons, with an internationally competitive catalog.
APPROACH
Every product begins with a clinical idea. We design it, certify it, and bring it to the operating room.
MARKET
We are present in Italy and abroad, in Europe, the United States, Latin America, and Asia, with a network of selected distributors.
The Civate (LC) plant is the heart of BRM production.
The Civate (LC) plant is the heart of BRM production.
Present on the Italian and international markets with a comprehensive portfolio of surgical medical devices for orthopedics, BRM Extremities meets the needs of public and private hospitals. Our range covers the key segments of extremity surgery : foot, hand, and trauma.
Cannulated screws for osteosynthesis, silicone spacers for MTF1, endortheses for flat feet and drills for percutaneous surgery.
Silicone spacers for the MCP and PIP joints. Cannulated screws for osteosynthesis of the wrist, scaphoid, metacarpals, and phalanges.
Cannulated headless screws for the fixation of bone fragments of various sizes.
BRM Extremities is more than just a manufacturer: we are a technology partner for orthopedic surgery. Each of our medical devices is created in our laboratories through a structured process that puts the surgeon and patient safety first.
design
We collaborate directly with internationally renowned surgeons to transform real operating room needs into effective solutions.
materials
Titanium Ti6Al4V for strength and biocompatibility, PEEK for radiolucency, latest generation silicones for elasticity.
TEST
Each device undergoes specific mechanical tests in accredited laboratories, in full compliance with international standards.
Our devices are approved for sale in Europe, the United States, South America, and Asia. Our expertise in CE, FDA, and ANVISA allows us to meet every type of request in the field of trauma and short-bone joint surgery, ensuring the highest standards of device quality and efficacy and patient safety.
No. We operate internationally with a network of selected distributors in Europe, the United States, Latin America, and Asia. Our devices are CE, FDA, and ANVISA certified.
Yes. BRM Extremities operates in full compliance with the European Medical Device Regulation and maintains up-to-date ISO 13485 and ISO 9001 certifications.
We accept proposals from specialist surgeons. Contact us using the form: our team will evaluate your idea and respond within 2 business days.
Fill out the form. We’ll get back to you within 2 business days.
