Mobarn Medical Devices, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mobarn Medical Devices, LLC - FDA 510(k) Cleared Devices
Recent clearances: Mobarn 80:20 Lumbar Interbody Fusion System (Posterior Lumbar Interbody Fusion Cage (PLIF))
1
Total
1
Cleared
0
Denied
Mobarn Medical Devices, LLC has 1 FDA 510(k) cleared medical devices. Based in New Orleans, US.
Latest FDA clearance: Sep 2025. Active since 2025. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Mobarn Medical Devices, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hypoid Ventures, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Mobarn Medical Devices, LLC
1 devices