Genesis Fracture Care, Inc. is one of 18463 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Genesis Fracture Care, Inc. - FDA 510(k) Cleared Devices
Recent clearances: G3™ Active Plate® Miniature System, G3(TM) Active Plate(R) Small Fragment System, G3¿ Active Plate® Large Fragment System
5
Total
5
Cleared
0
Denied
Genesis Fracture Care, Inc. has 5 FDA 510(k) cleared medical devices. Based in Clackamas, US.
Historical record: 5 cleared submissions from 2014 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Genesis Fracture Care, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Memphis Regulatory Consulting, LLC and Mrc-X, LLC.
FDA 510(k) Regulatory Record - Genesis Fracture Care, Inc.
5 devices
Cleared
Oct 23, 2017
G3™ Active Plate® Miniature System
Orthopedic
174d
Cleared
Apr 22, 2016
G3(TM) Active Plate(R) Small Fragment System
Orthopedic
46d
Cleared
Nov 24, 2015
G3¿ Active Plate® Large Fragment System
Orthopedic
106d
Cleared
Apr 30, 2015
G3 Active Plate Large Fragment System
Orthopedic
49d
Cleared
Nov 26, 2014
G3 Active Plate Large Fragment System
Orthopedic
48d