Met One Technologies is one of 13015 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Met One Technologies - FDA 510(k) Cleared Devices
Recent clearances: AUDERE Lumbar Spacer System, Met One Czar Anterior Cervical Plate System, Xultan 5.5 Pedicle Screw System
3
Total
3
Cleared
0
Denied
Met One Technologies has 3 FDA 510(k) cleared medical devices. Based in El Paso, US.
Historical record: 3 cleared submissions from 2017 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Met One Technologies Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Empirical Testing Corp and Jalex Medical, LLC.
FDA 510(k) Regulatory Record - Met One Technologies
3 devices