Ellipse Technologies, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Ellipse Technologies, Inc. has 13 FDA 510(k) cleared orthopedic devices. Based in Irvine, US.
Historical record: 13 cleared submissions from 2011 to 2016.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
13 devices
Cleared
Apr 04, 2016
PRECICE Intramedullary Limb Lengthening System
Orthopedic
59d
Cleared
Mar 24, 2015
MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
Orthopedic
312d
Cleared
Oct 07, 2014
RESIDUAL LIMB LENGTHENING SYSTEM
Orthopedic
102d
Cleared
Sep 18, 2014
MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
Orthopedic
192d
Cleared
Jun 30, 2014
PRECICE TRAUMA NAIL SYSTEM
Orthopedic
28d
Cleared
May 20, 2014
PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
Orthopedic
29d
Cleared
Feb 27, 2014
ELLIPSE MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
Orthopedic
34d
Cleared
Jan 23, 2014
ELLIPSE PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
Orthopedic
245d
Cleared
Dec 09, 2013
PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
Orthopedic
45d
Cleared
Oct 11, 2013
PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
Orthopedic
123d
Cleared
Oct 19, 2012
ELLIPSE PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
Orthopedic
353d
Cleared
Mar 28, 2012
ELLIPSE PRECICE TRAUMA NAIL SYSTEM
Orthopedic
103d
Cleared
Jul 12, 2011
ELLIPSE INTRAMEDULLARY LIMB LENGTHENING SYSTEM
Orthopedic
362d