Kinamed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kinamed, Inc. - FDA 510(k) Cleared Devices
33
Total
29
Cleared
0
Denied
Kinamed, Inc. has 29 FDA 510(k) cleared orthopedic devices. Based in Los Angeles, US.
Historical record: 29 cleared submissions from 1988 to 2013.
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 - Kinamed, Inc.
33 devices
Cleared
Apr 05, 2013
NEUROPRO LOW PROFILE CRANIAL PLATING SYSTEM
Neurology
267d
Cleared
Nov 09, 2007
SUPERCABLE GRIP AND PLATE SYSTEM
Orthopedic
88d
Cleared
May 24, 2005
NAVIPRO SHOULDER SOFTWARE MODULE
Neurology
46d
Cleared
Mar 11, 2004
NAVIPRO KNEE SOFTWARE MODULE
Neurology
111d
Cleared
Dec 19, 2003
GEM INSET PATELLAR COMPONENT
Orthopedic
88d
Cleared
Oct 21, 2003
ISO-ELASTIC CERCLAGE SYSTEM
Orthopedic
270d
Cleared
Jun 03, 2002
NAVIPRO
Neurology
88d
Cleared
May 21, 2002
KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT
Orthopedic
169d
Cleared
May 17, 2001
GEM POSTERIOR STABILIZED TOTAL KNEE SYSTEM
Orthopedic
126d
Cleared
Feb 23, 2001
ORTHOPILOT
Neurology
121d
Cleared
Jul 19, 2000
GEM KNEE SYSTEM
Orthopedic
218d
Cleared
Sep 08, 1998
QUICK TAP SELF DRILLING SCREW
Dental
19d