Relja Innovations, LLC is one of 19261 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Relja Innovations, LLC - FDA 510(k) Cleared Devices
Recent clearances: Lapidus Screw Kit, MIS Precision Chevron Bunion System
2
Total
2
Cleared
0
Denied
Relja Innovations, LLC has 2 FDA 510(k) cleared medical devices. Based in Brookfield, US.
Latest FDA clearance: Jul 2026. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Relja Innovations, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Acknowledge Regulatory Strategies, Inc. and MRC Global.
FDA 510(k) Regulatory Record - Relja Innovations, LLC
2 devices