Alliance Partners, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alliance Partners, LLC - FDA 510(k) Cleared Devices
Recent clearances: Medina Anterior Cervical Plate System, Alamo® C
10
Total
10
Cleared
0
Denied
Alliance Partners, LLC has 10 FDA 510(k) cleared orthopedic devices. Based in Avon Lake, US.
Historical record: 10 cleared submissions from 2011 to 2020.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Testing Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Alliance Partners, LLC
10 devices
Cleared
Aug 06, 2020
Medina Anterior Cervical Plate System
Orthopedic
59d
Cleared
Mar 22, 2018
Alamo® C
Orthopedic
174d
Cleared
Feb 27, 2015
ALLIANCE SPINE RAAS CRANIAL PLATING SYSTEM
Neurology
302d
Cleared
Nov 06, 2014
NAKOMA ACP
Orthopedic
107d
Cleared
Apr 21, 2014
ALAMO T
Orthopedic
74d
Cleared
Jan 09, 2014
ALAMO C
Orthopedic
72d
Cleared
Oct 05, 2012
ALAMO T
Orthopedic
240d
Cleared
Sep 04, 2012
ALAMO P
Orthopedic
54d
Cleared
Aug 22, 2012
SWANNSHIDI BONE MARROW ASPIRATION NEEDLE
Gastroenterology & Urology
126d
Cleared
Nov 30, 2011
ALAMO C
Orthopedic
105d