Reliance Medical Systems, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reliance Medical Systems, LLC - FDA 510(k) Cleared Devices
Recent clearances: Reliance Cervical IBF System, Reliance Spinal Screw System, Reliance Lumbar IBF System
24
Total
24
Cleared
0
Denied
Reliance Medical Systems, LLC has 24 FDA 510(k) cleared orthopedic devices. Based in Sandy, US.
Last cleared in 2022. Active since 2007.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Reliance Medical Systems, LLC
24 devices
Cleared
Mar 29, 2022
Reliance Cervical IBF System
Orthopedic
595d
Cleared
May 13, 2021
Reliance Spinal Screw System
Orthopedic
50d
Cleared
Feb 15, 2019
Reliance Lumbar IBF System
Orthopedic
105d
Cleared
Jan 19, 2018
Reliance Lumbar IBF System
Orthopedic
95d
Cleared
Dec 29, 2017
Reliance Cervical IBF System
Orthopedic
91d
Cleared
Sep 07, 2017
Reliance Cervical IBF System
Orthopedic
21d
Cleared
Dec 02, 2016
Reliance Spinal Screw System
Orthopedic
129d
Cleared
May 20, 2016
Reliance Lumbar IBF System
Orthopedic
91d
Cleared
Sep 17, 2015
Reliance Spinal Screw System
Orthopedic
48d
Cleared
Jun 09, 2015
Reliance Cervical IBF System
Orthopedic
298d
Cleared
Apr 29, 2015
Reliance Posterior Cervical-Thoracic System
Orthopedic
210d
Cleared
Apr 02, 2015
Reliance Interspinous Plate System
Orthopedic
233d