Wednesday, October 11, 2023
TechMah CMF LLC, an innovative medical technology company, is excited to announce that its groundbreaking medical device, the tmCMF Solution, has received FDA 510(k) approval. This regulatory clearance represents a significant achievement for the company, underscoring its commitment to advancing healthcare through cutting-edge technology.
The tmCMF Solution is a comprehensive suite of customized product offerings designed for trauma and reconstruction procedures in the mandible and midface. It comprises the innovative Surgeon Review Tool (SRT) software and a range of maxillofacial and mandibular surgical instruments, including surgical guides, anatomical models, and dental splints. Notably, these surgical instruments are tailored to each patient, meticulously crafted using CT and dental scan data.
The SRT software is the core of this solution, serving as an intuitive, surgeon-driven digital tool that seamlessly integrates patient-centered healthcare with artificial intelligence. This results in tailored preoperative plans and the production of precise 3D-printed surgical instruments, benefitting surgeons and patients worldwide.
The tmCMF Solution is set to transform the field of maxillofacial and mandibular surgery, providing a vital preoperative tool for simulating and evaluating surgical procedures, giving surgeons greater accuracy and confidence in their work. with the tmCMF Solution poised to set new standards in craniomaxillofacial reconstructive surgery, ultimately improving patient care and outcomes.
Source: prnewswire.com
