Meduloc, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Meduloc, LLC - FDA 510(k) Cleared Devices
Recent clearances: Meduloc Intramedullary Fracture Fixation (IFF) System
1
Total
1
Cleared
0
Denied
Meduloc, LLC has 1 FDA 510(k) cleared medical devices. Based in Del Mar, US.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Meduloc, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Meduloc, LLC
1 devices