The MEDICREA® Group announced that it has received FDA-Clearance for TULIP GENESIS™ which completes its UNiD™ ASI platform technology. With the FDA clearance of the TULIP GENESIS™, MEDICREA® completes its UNiD™ ASI platform by providing a top loading screw solution designed to integrate seamlessly with UNiD™ ASI. TULIP GENESIS™ is a comprehensive top loading screw system that competes with any screw system on the market offering solutions for both degen and complex deformity cases. It is the only FDA-cleared top loading screw system that can be used with the uniqueUNiD™ ROD. MEDICREA® ’s implant database integrated within the UNiD™ HUB now includes: IB3D™, a selection of 3D-printed patient-specific interbody cages; UNiD™ ROD, a patient-specific rod industrially pre-bent to precisely match the optimal individual surgical simulation; PASS LP™, a modular screw system; and TULIP GENESIS™, a top-loading screw system. MEDICREA® ’s proprietary UNiD™ ASI technology is a comprehensive suite of solutions comprising services and products designed to help surgeons improve their patient’s outcomes. By leveraging artificial intelligence and the latest clinical research, the platform enables the surgeon to plan cases preoperatively. The Artificial Intelligence embedded within the platform allows a surgeon to visualize the compensatory mechanisms above and below the instrumented spine that will most likely occur based on their surgical plan. This unique technology offers solutions designed both for complex deformity and degenerative applications. The combination of A.I. with this product offering makes MEDICREA® the only manufacturer able to streamline inventory required to operate as well as provide patient-specific devices, through intelligent pre-operative surgical planning. The MEDICREA® ’s UNiD™ LAB team of biomedical engineers can more efficiently generate comprehensive surgical plans, using outcome-centered predictive modeling algorithms to optimize surgical strategy. These documented UNID™ surgical plans also allow the operating room staff to clearly anticipate when each implant will be needed by the surgeon. This is a critical combination as it streamlines the OR workflow with precise pre-selected implants and alignment of staff to the patient specific surgical plan and as it makes the surgery safer for the patient by reducing the chances for errors.