Category: Surgery

Unify Medical Announces CRADA Agreement With U.S. Special Operations Command
Press Release Aug 23, 2023
Unify Medical Announces CRADA Agreement With U.S. Special Operations Command
Nexxt Spine Announces Early Significant Clinical Evidence Results and Completes Enrollment for NEXXT MATRIXX 3-D Printed Technologies
Press Release Jul 12, 2022
Nexxt Spine Announces Early Significant Clinical Evidence Results and Completes Enrollment for NEXXT MATRIXX 3-D Printed Technologies
NGMedical GmbH Announces First Case of Its BEE PLIF in the USA
Press Release Feb 23, 2022
NGMedical GmbH Announces First Case of Its BEE PLIF in the USA
NGMedical, Inc. Announces the Appointment of Mitch White as President and General Manager of its United States' Business
Press Release Jan 20, 2022
NGMedical, Inc. Announces the Appointment of Mitch White as President and General Manager of its United States' Business
NGMedical GmbH Receives FDA Clearance for Its AM Titanium Lumbar Interbody BEE® PLIF
Press Release Sep 27, 2021
NGMedical GmbH Receives FDA Clearance for Its AM Titanium Lumbar Interbody BEE® PLIF

NGMedical announces the clearance of its third spinal implant this year.
Empirical Spine Closes $10 Million Series B Financing
Press Release Jun 2, 2021
Empirical Spine Closes $10 Million Series B Financing

LimiFlex Paraspinous Tension Band on track for PMA Submission
Curiteva Adds Steve Cichy as Strategic Advisor and Erik Erbe, PhD, as Vice President of Clinical and Research
Press Release Apr 28, 2021
Curiteva Adds Steve Cichy as Strategic Advisor and Erik Erbe, PhD, as Vice President of Clinical and Research

Curiteva adds two additional industry experts to help strategically lead the company and the development of its novel technology for the medical device industry
Empirical Spine Receives FDA Breakthrough Device Designation for the Limiflex Device Targeting Degenerative Spondylolisthesis
Press Release Apr 1, 2021
Empirical Spine Receives FDA Breakthrough Device Designation for the Limiflex Device Targeting Degenerative Spondylolisthesis

The Breakthrough Devices Program is a voluntary program for certain medical devices and device-led combination products that provide for more effective treatment or diagnosis of life-threatening or irreversibly debilitating diseases or conditions.
NGMedical GmbH Receives FDA Clearance for Its BEE® HA Cervical Cage System Made From PEEK-OPTIMATM HA Enhanced
Press Release Mar 30, 2021
NGMedical GmbH Receives FDA Clearance for Its BEE® HA Cervical Cage System Made From PEEK-OPTIMATM HA Enhanced

BEE® HA was developed to optimize fusion, while maintaining elasticity that is similar to bone and radiolucency of the cage body.
Empirical Spine Initiates PMA Submission Process for FDA Approval of Limiflex for Degenerative Spondylolisthesis
Press Release Feb 25, 2021
Empirical Spine Initiates PMA Submission Process for FDA Approval of Limiflex for Degenerative Spondylolisthesis

The LimiFlex Paraspinous Tension Band is a new, investigational device designed as an alternative to spinal fusion for patients receiving surgical decompression for grade 1 lumbar degenerative spondylolisthesis with spinal stenosis.
NGMedical GmbH Receives FDA Clearance for Its AM Titanium Cervical Interbody BEE®
Press Release Feb 3, 2021
NGMedical GmbH Receives FDA Clearance for Its AM Titanium Cervical Interbody BEE®

NGMedical achieves milestone with first FDA clearance for its innovative spinal implants.