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MoRe® News

Press Releases

February 23, 2021

MiRus® Launches MoRe® Promise- a Lifetime Limited Warranty for its Molybdenum-Rhenium Superalloy Rod.

MiRus announced today that they will offer a LIFETIME LIMITED WARRANTY on its Molybdenum-Rhenium ( MoRe®) superalloy rod technology. The warranty will cover full replacement of the MoRe® Rod and corresponding MiRus hardware used in spinal fusion cases should the MoRe® Rod fracture. The warranty will cover all thoracolumbar MoRe® rods implanted as part of the EUROPA™ Pedicle Screw System supplied by MiRus in the United States effective March 1, 2021.
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June 11, 2020

MiRus® Announces First Clinical Use of the MiRus® 3DR™ Printed Lumbar Interbody Fusion System.

MiRus is pleased to announce that it received FDA 510(k) clearance for its 3DR™ (Randomized) Printed Lumbar Interbody Fusion System which consists of the CALLISTO 3DR™ PLIF, HYPERION 3DR™ TLIF, CALYPSO 3DR™ LLIF and the ANTARES 3DR™ ALIF.
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August 30, 2019

First Spine Surgeries using the MoRe® Superalloy.

MiRus announces successful spine surgeries at several centers across the country using the MoRe® superalloy. MiRus had received FDA 510(k) clearance for the MoRe® based Europa™ Pedicle Screw System earlier this year.
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July 26, 2019

MiRus® Receives FDA Clearance for Lowest Profile Anterior Cervical Plate System.

MiRus is pleased to announce recent FDA 510(k) clearance of the CYGNUS™ Anterior Cervical Plate System, the narrowest and thinnest cervical plate on the market.
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July 22, 2019

First System for Dynamic Intra-operative Measurement of Segmental and Global Spine Alignment Receives FDA Clearance.

MiRus is pleased to announce FDA 510(k) clearance of the GALILEO™ Spine Alignment Monitoring System, a non-optical, wireless, real-time measurement system for segmental and global sagittal spine alignment.
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June 24, 2019

MiRus Aquires 50,000 SQFT Manufacturing Facility.

Following the 510(k) clearance by FDA in March 2019 of MoRe®, a proprietary molybdenum rhenium superalloy for medical implants, MiRus is excited to announce a major expansion of its manufacturing capacity with the addition of a fully operational 50,000 sqft orthopaedic and spine manufacturing plant in Marietta, GA.
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March 27, 2019

MiRus Receives FDA 510(k) Approval for First Medical Implant with New Superalloy.

MiRus has received FDA 510(k) approval for the MoRe® based Europa™ Pedicle Screw System making it the first FDA approved medical device with this new class of implant material.
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September 17, 2018

MiRus™ Wins Two 2018 Spine Technology Awards

For Immediate Release Atlanta – September 17, 2018– MiRus™ Wins Two 2018 Spine Technology Awards Winning Multiple Awards in One Year, MiRus Takes Honors for EUROPA™ Pedicle Screw System and GALILEO™ Spine Alignment Monitoring System MiRus has won the Annual Spine Technology Awards for both of its initial products in the implant and navigation categories. The Spine Technology Awards are …

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The Latest from MiRus

MiRus Receives New Technology Add-on Payment (NTAP) for EUROPA™ Posterior Cervical Fusion System

August 1, 2025

MiRus Siegel™ TAVR US Early Feasibility Study (EFS) 30 Day Results Presented at NY Valves Meeting

July 2, 2025

MiRus Siegel™ TAVR: First EFS Cases

March 28, 2025

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July 31, 2024
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