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Latest from EXALTA

Company news, industry insights, events, and announcements shaping the future of EXALTA.

  1. A lab technician works at an EXALTA biosafety cabinet with text announcing EXALTA's ISO 17025 Microbiology Lab Accreditation to strengthen capabilities for MedTech innovators. Apr 22, 2026 Press Release EXALTA Strengthens MedTech Development with ISO 17025 Microbiology Laboratory Accreditation The accreditation adds in-house microbiology testing to EXALTA's connected development, regulatory, and manufacturing model, supporting faster paths to market.
  2. Mar 3, 2026 Press Release EXALTA Achieves EU-MDR Certification to Support Plating & Cable Fixation, Supporting Customer Growth Across Europe
  3. EXALTA Group Receives FDA 510(k) Clearance for New Anterior Cervical Plating System Nov 13, 2025 Press Release EXALTA Group Receives FDA 510(k) Clearance for New Anterior Cervical Plating System EXALTA Group, a next-generation partner to MedTech innovators, today announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for its Anterior Cervical Plating (ACP) System, designed to support stability and fusion in the cervical spine.
  4. Accelerating Medtech Innovation Through Integrated Solutions—An Orthopedic Innovators Q&A Nov 7, 2025 Article Accelerating Medtech Innovation Through Integrated Solutions—An Orthopedic Innovators Q&A The orthopedic market is changing at the clinical level. The increasing role of ASCs, influx of robotic-based solutions, and growing interest in single-use, sterile packaged instrumentation have created a need for product innovation. In response, orthopedic device OEMs are seeking assistance from their design and manufacturing partners to help develop and launch new systems.
  5. EXALTA Secures EU-MDR Certification for Titanium Compression Screws, Expanding Access to Advanced Trauma Solutions Oct 16, 2025 Press Release EXALTA Secures EU-MDR Certification for Titanium Compression Screws, Expanding Access to Advanced Trauma Solutions EXALTA Group, a global leader in the development and manufacturing of integrated OEM solutions for mission-critical medical devices, today announced it has obtained European Medical Device Regulation (EU-MDR) certification for its full range of headed and headless titanium compression screws used in trauma and reconstructive surgery.
  6. A September marked by conviviality and sharing Oct 10, 2025 Article A September marked by conviviality and sharing On Friday, September 12, we had the honor of officially inaugurating our new factory in Rang-du-Fliers, in the presence of Mohamed Chakroun, our Group Operations Director, who performed the traditional ribbon cutting ceremony.
  7. Sep 12, 2025 Press Release Introducing EXALTA: A Bold New Brand Unifying Intech, Tyber and Resolve to Accelerate the Future of MedTech Intech, Tyber Medical, and Resolve Surgical Technologies are proud to announce their rebrand under a unified identity: EXALTA. This transformation brings together three industry pioneers under one banner, reinforcing a shared objective: advancing the future of MedTech with greater clinical impact and improved patient outcomes.
  8. EXALTA Achieves EU-MDR Certification for Trauma Plating System, Building Momentum After Recent Screw Portfolio Approval May 1, 2025 Press Release EXALTA Achieves EU-MDR Certification for Trauma Plating System, Building Momentum After Recent Screw Portfolio Approval EXALTA Achieves EU-MDR Certification for Trauma Plating System, Building Momentum After Recent Screw Portfolio Approval