FOX8 Cleveland

CE Mark Approval for RemeOs™ Trauma Screw Product Group, featuring four product lines with over 200 individual products, drives global expansion for Bioretec

TAMPERE, Finland, Feb. 14, 2025 /PRNewswire/ -- Bioretec Ltd., a pioneer in absorbable orthopedic implants, has achieved a pivotal milestone with the successful completion of its CE mark approval ...
WRBL

The commercialization of Bioretec's RemeOs™ Trauma Screw in the U.S. proceeds with the signing of new logistics agreement

Bioretec is a globally operating Finnish medical device company that continues to pioneer the application of biodegradable orthopedic implants. The company has built unique competencies in the ...
Healio

Tyber Medical issued 510(k) clearance for trauma screw system

We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. Back to Healio Tyber Medical recently announced it has ...
Healio

Bioretec receives FDA market authorization for RemeOs trauma screw

Please provide your email address to receive an email when new articles are posted on . Bioretec has received FDA market authorization for its RemeOs trauma screw. The bioresorbable metal implant is ...
Morningstar

Bioretec Ltd's business review January-September 2024: Launch of the RemeOs™ Trauma Screw in the U.S. is proceeding to the next phase, EU authorization in the final stage

Alan Donze, CEO of Bioretec Ltd: " As I reflect on my first 100 days as CEO, I am both proud of the strides we have made and energized by the opportunities ahead for Bioretec. Our commitment to ...
FOX8 Cleveland

FDA approves Bioretec's RemeOs™ trauma screw as the first bioresorbable metal implant in the U.S. market

The benefits of the RemeOs™ trauma screw have been validated in clinical trials and have already previously been recognized by the FDA granting the Breakthrough Device Designation. Bioresorbable ...