Elute, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Elute, Inc. has 2 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Latest FDA clearance: Feb 2025. Active since 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Elute, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Elute, Inc.
2 devices