Ellipse Technologies, Incorporated - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Ellipse Technologies, Incorporated has 7 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 7 cleared submissions from 2015 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Ellipse Technologies, Incorporated Filter by specialty or product code using the sidebar.
7 devices
Cleared
Mar 31, 2016
PRECICE Trauma Nail System
Orthopedic
58d
Cleared
Jan 25, 2016
Ellipse Supplemental Instrument Trays
General Hospital
227d
Cleared
Dec 22, 2015
PRECICE Trauma Nail System
Orthopedic
123d
Cleared
Jun 19, 2015
PRECICE Intramedullary Limb Lengthening System
Orthopedic
52d
Cleared
May 29, 2015
MAGEC 2 Spinal Bracing and Distraction System
Orthopedic
57d
Cleared
Apr 23, 2015
PRECICE Intramedullary Limb Lengthening System
Orthopedic
41d
Cleared
Jan 16, 2015
PRECISE Trauma Nail System
Orthopedic
123d