Company intelligence / Profile preview

ZSFab

Waltham, Massachusetts, United Stateszsfab.com ↗

Ownership: Private
Development stage: Commercial

Overview

ZSFab has received FDA 510(k) clearance for its first cervical fusion cage in January 2021 and its first lumbar interbody system in October 2022. The company’s InterConnect™ Lumbar Interbody System and Cervical Interbody System have been successfully used clinically in the US, with prior clinical use of the cervical system also reported in China. These devices feature advanced porous titanium lattice structures designed to enhance osseointegration, reduce subsidence, improve load distribution, and promote faster bone healing.

Therapeutic areas: Neurology
Modalities: Device3D printed implant (Additively manufactured device)
Industry: Implantable Medical Devices

Drug pipeline

1 asset

InterConnect 3D Printed Ti Lumbar Interbody System

Commercial

Indications: Spinal fusion

Partnerships

Dr. Fernando Villamil at CORE HospitalDrs. Daniel Harwell and Michael Thambuswamy at Oklahoma Spine & Brain Institute

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