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

FDA 510(k) Regulatory Record - Kinamed, Inc. Orthopedic ✕

27 devices

1-12 of 27

Cleared Nov 09, 2007

SUPERCABLE GRIP AND PLATE SYSTEM

Orthopedic · 88d

Cleared Dec 19, 2003

GEM INSET PATELLAR COMPONENT

Orthopedic · 88d

Cleared Oct 21, 2003

ISO-ELASTIC CERCLAGE SYSTEM

Orthopedic · 270d

Cleared May 21, 2002

KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT

Orthopedic · 169d

Cleared May 17, 2001

GEM POSTERIOR STABILIZED TOTAL KNEE SYSTEM

Orthopedic · 126d

Cleared Jul 19, 2000

GEM KNEE SYSTEM

Orthopedic · 218d

Cleared Jan 16, 1997

KINAMED PROFIX SYSTEM

Orthopedic · 76d

Cleared Dec 04, 1995

REALITY LONG STEM HIP SYSTEM

Orthopedic · 87d

Cleared Oct 25, 1995

ATH FULL PROFILE ACETABULAR CUP SYSTEM

Orthopedic · 48d

Cleared Mar 30, 1994

KINAMED REALITY TOTAL HIP SYSTEM

Orthopedic · 686d

Cleared Nov 03, 1992

KINAMED 32MM BIOCERAM-Z TOATAL HIP FEMORAL BALL

Orthopedic · 286d

Cleared Oct 30, 1992

KINAMED 26MM BIOCERAN-Z TOTAL HIP FEMORAL BALL

Orthopedic · 288d