Duet Spine Holdings, LLC is one of 16117 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Duet Spine Holdings, LLC - FDA 510(k) Cleared Devices
Recent clearances: Duet™ Spinal Fixation System
1
Total
1
Cleared
0
Denied
Duet Spine Holdings, LLC has 1 FDA 510(k) cleared medical devices. Based in Winona Lake, US.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Duet Spine Holdings, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ATS Colorado Springs as regulatory consultant.
FDA 510(k) Regulatory Record - Duet Spine Holdings, LLC
1 devices