HD LifeSciences Receives 510(k) Clearance for Hive™ ALIF Standalone System

May 12, 2020

Updated: Feb 2, 2021 – HD LifeSciences has received 510(k) clearance from the U.S Food and Drug Administration (FDA) for its Hive(tm) ALIF Standalone Lumbar Interbody Fusion System. The patented implant system features a modular anterior portion that allows surgeon choice and flexibility in using integrated zero-profile fixation or anterior plating. The implant also features a patent-pending mechanism that allows the surgeon to adjust the footprint of the device pre-implantation to better match patient anatomy.

NanoHive Medical, LLC is a pioneer and leading innovator in 3D printed spinal interbody fusion implants and instrumentation. The company’s proprietary, biomimetic Soft Titanium® technology clearly distinguishes their products in the $1.9B spinal interbody fusion device market. The Hive™ portfolio of interbody fusion devices provide surgeons and their patients ideal biomechanical elastic modulus properties, clear and precise diagnostic imaging capability, osteoblast cell attraction and integration – all features that lead to consistently strong fusion constructs and efficacious clinical experiences.

NanoHive Medical is located in Woburn, Massachusetts U.S.A.

Contact: Patrick O’Donnell, CEO & President at Patrick.odonnell@nanohive.com

Website: www.nanohive.com