K Line Europe, a leading manufacturer of OEM Clear Aligners in Europe, has received FDA registration to introduce its popular K Clear Aligners in the United States. The company’s low refinement rate of 15.8% sets it apart from competitors, ensuring more predictable case outcomes, increased patient satisfaction, and higher productivity for practitioners.
Unlike other companies, K Line Europe achieves its industry-leading refinement rate through a unique process involving a team of expert orthodontists and dentists. Operating from its advanced facility in Germany, K Line manufactures 7,000 aligners daily, using its proprietary K Flex material. This material offers enhanced patient comfort, durability, and predictable movement.
To streamline the submission process, K Line Europe provides a user-friendly submission portal that is compatible with all 3D IO Scanners and generates a universal STL file. The submission portal is free of charge, allowing practitioners to easily submit their cases. Once a case is submitted, aligners are manufactured within 3-5 days and shipped overnight to the newly opened distribution center in Florida. From there, they are boxed and shipped to the clinic at no additional cost. The entire process typically takes an average of 14-16 days, ensuring a quick turnaround time for practitioners and patients.
In the near future, K Line products will be available through most full-service dental dealers, making them easily accessible to dental professionals across the country. Additionally, K Line offers private label opportunities to dealers, groups, and DSOs, providing a customizable option for those looking to offer their own branded aligners.
For more information on K Line’s Clear Aligners and how to access them, individuals can contact their authorized K Line dealer or visit the company’s website at www.k-lineus.com. K Line Europe’s entry into the US market brings a new option for practitioners and patients seeking high-quality clear aligners with a proven track record of success.