Extremities Regulatory Top Stories CE Mark Approval for RemeOs™ Trauma Screw Product Group, featuring four product lines with over 200 individual products, drives global expansion for Bioretec byBree MillerFebruary 14, 2025
Extremities Regulatory Inside information: Bioretec Ltd. receives CE mark approval for RemeOs™ Trauma Screw product portfolio, allowing market launch in Europe byTim AllenJanuary 31, 2025
Extremities The commercialization of Bioretec’s RemeOs™ Trauma Screw in the U.S. proceeds with the signing of new logistics agreement byJosh SandbergNovember 20, 2024
Extremities Forma Medical Announces Milestone Achievement: 15th Patient Successfully Treated with OptimalMTP®, the World’s First Minimally Invasive Plate and Screw System byTim AllenSeptember 6, 2024
Extremities Bioretec reports successful clinical outcomes from U.S. controlled launch of RemeOs™ trauma screw: fracture healing confirmed in 100% of surgical procedures byTim AllenJune 19, 2024
Extremities Top Stories Medline to launch Lisfranc System at ACFAS 2024 Annual Scientific Conference byJosh SandbergJanuary 30, 2024
Extremities Regulatory Tyber Medical Receives FDA Clearance on Plating System Line Extension byJosh SandbergJanuary 29, 2024
Extremities Regulatory Top Stories Bioretec is the first in the world to receive FDA approval for a bioresorbable metal product byJosh SandbergMarch 30, 2023
Regulatory Top Stories Bioretec updates its estimate of the timing for approval of the CE mark for the RemeOs™ trauma screw byJosh SandbergNovember 4, 2022
Extremities Regulatory Top Stories Bioretec updates estimate of U.S. registration of RemeOs™ screws and expects approval in April 2023 byJosh SandbergOctober 14, 2022
