Cymedica Orthopedics, Inc. is one of 16470 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cymedica Orthopedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Motive™ Electrode, Motive Knee Wrap, Intellihab System
5
Total
5
Cleared
0
Denied
Cymedica Orthopedics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Scottsdale, US.
Last cleared in 2023. Active since 2015. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Cymedica Orthopedics, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Third Party Review Group, LLC and Regulatory Technology Services, LLC. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Cymedica Orthopedics, Inc.
5 devices
Cleared
Mar 22, 2023
Motive™ Electrode
Neurology
23d
Cleared
May 12, 2022
Motive Knee Wrap
Physical Medicine
59d
Cleared
CT
Jun 03, 2021
Intellihab System
Physical Medicine
94d
Cleared
Dec 01, 2016
CyMedica e-vive™ System
Physical Medicine
29d
Cleared
Apr 02, 2015
QB1 System Powered Muscle Stimulator & Transcutaneous Electrical Nerve...
Physical Medicine
43d