New Standard Device Dba Metalogix - FDA 510(k) Cleared Devices
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.
2 devices