Ulrich Medical USA is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ulrich Medical USA - FDA 510(k) Cleared Devices
Recent clearances: Momentum® Posterior Spinal Fixation System with G21 V-STEADY Bone Cement, Cortium™, Momentum® MIS Posterior Spinal Fixation System
8
Total
8
Cleared
0
Denied
Ulrich Medical USA has 8 FDA 510(k) cleared medical devices. Based in Chesterfield, US.
Last cleared in 2023. Active since 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Ulrich Medical USA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ulrich Medical USA
8 devices
Cleared
Oct 20, 2023
Momentum® Posterior Spinal Fixation System with G21 V-STEADY Bone Cement
Orthopedic
122d
Cleared
May 02, 2023
Cortium™
Orthopedic
57d
Cleared
Nov 28, 2022
Momentum® MIS Posterior Spinal Fixation System
Orthopedic
35d
Cleared
Aug 19, 2022
uCerv Flux-C 3D Porous Titanium Cervical Interbody
Orthopedic
163d
Cleared
Sep 10, 2020
Navigation Module of the Momentum System
Orthopedic
163d
Cleared
Oct 02, 2019
Momentum™ Posterior Spinal Fixation System
Orthopedic
75d
Cleared
Nov 16, 2018
Solidity Vertebral Body Replacement
Orthopedic
121d
Cleared
Jun 22, 2015
uNion Cervical Plate System
Orthopedic
98d