Understand the Nuance
Published loading...Updated

Curiteva® Secures FDA 510(k) Clearance for Inspire® Trabecular PEEK Standalone ALIF System – Ortho Spine News

Summary by Ortho Spine News | Your Trusted Voice for Medical Device Industry Ortho News
Huntsville, AL., (June 24, 2025) – Curiteva is proud to announce FDA 510(k) clearance for the Inspire Trabecular PEEK Standalone ALIF system, the first-ever 3D printed PEEK standalone implant. This is the company’s latest FDA cleared 3D Printed PEEK implant with HAFUSE technology. This milestone represents a significant leap forward in advanced medical solutions and further solidifies Curiteva’s position as a leader in healthcare innovation.   “T
DisclaimerThis story is only covered by news sources that have yet to be evaluated by the independent media monitoring agencies we use to assess the quality and reliability of news outlets on our platform. Learn more here.

Bias Distribution

  • There is no tracked Bias information for the sources covering this story.
Factuality

To view factuality data please Upgrade to Premium

Ownership

To view ownership data please Upgrade to Vantage

Ortho Spine News | Your Trusted Voice for Medical Device Industry Ortho News broke the news in on Tuesday, June 24, 2025.
Sources are mostly out of (0)