New Standard Device Dba Metalogix is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
New Standard Device Dba Metalogix - FDA 510(k) Cleared Devices
Recent clearances: Revolution External Plating System, Revolution External Plating System
2
Total
2
Cleared
0
Denied
New Standard Device Dba Metalogix has 2 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Latest FDA clearance: May 2024. Active since 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by New Standard Device Dba Metalogix Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - New Standard Device Dba Metalogix
2 devices