Orbbo Surgical, LLC is one of 18441 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orbbo Surgical, LLC - FDA 510(k) Cleared Devices
Recent clearances: Kepler II, Kepler I Cervical Plate System, Hubble I System
4
Total
4
Cleared
0
Denied
Orbbo Surgical, LLC has 4 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 4 cleared submissions from 2016 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orbbo Surgical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Novus Management Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Orbbo Surgical, LLC
4 devices