Medynus, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medynus, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IMPEACE and IMPEACE-Uni Anterior Cervical Plate System, Medynus IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage, Goblin and Goblin LS Pedicle Screw Systems
3
Total
3
Cleared
0
Denied
Medynus, Inc. has 3 FDA 510(k) cleared medical devices. Based in Irvine, US.
Last cleared in 2022. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Medynus, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Eerkie Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - Medynus, Inc.
3 devices