Medical Device Manufacturer · US , Los Angeles , CA

Kinamed, Inc. - FDA 510(k) Cleared Devices

33 submissions · 29 cleared · Since 1988
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
1-12 of 33
Cleared Apr 05, 2013
NEUROPRO LOW PROFILE CRANIAL PLATING SYSTEM
K122049 · GWO
Neurology · 267d
Cleared Nov 09, 2007
SUPERCABLE GRIP AND PLATE SYSTEM
K072250 · KTT
Orthopedic · 88d
Cleared May 24, 2005
NAVIPRO SHOULDER SOFTWARE MODULE
K050897 · HAW
Neurology · 46d
Cleared Mar 11, 2004
NAVIPRO KNEE SOFTWARE MODULE
K033668 · HAW
Neurology · 111d
Cleared Dec 19, 2003
GEM INSET PATELLAR COMPONENT
K032950 · JWH
Orthopedic · 88d
Cleared Oct 21, 2003
ISO-ELASTIC CERCLAGE SYSTEM
K030256 · JDQ
Orthopedic · 270d
Cleared Jun 03, 2002
NAVIPRO
K020764 · HAW
Neurology · 88d
Cleared May 21, 2002
KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT
K013982 · KRR
Orthopedic · 169d
Cleared May 17, 2001
GEM POSTERIOR STABILIZED TOTAL KNEE SYSTEM
K010101 · JWH
Orthopedic · 126d
Cleared Feb 23, 2001
ORTHOPILOT
K003347 · HAW
Neurology · 121d
Cleared Jul 19, 2000
GEM KNEE SYSTEM
K994214 · JWH
Orthopedic · 218d
Cleared Sep 08, 1998
QUICK TAP SELF DRILLING SCREW
K982927 · DZL
Dental · 19d
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