Richards Medical Co., Inc. - FDA 510(k) Cleared Devices
71
Total
59
Cleared
0
Denied
Richards Medical Co., Inc. has 59 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 59 cleared submissions from 1983 to 1990. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Richards Medical Co., Inc. Filter by specialty or product code using the sidebar.
71 devices
Cleared
Jun 25, 1990
ROGOZINSKI SPINAL SYSTEM, ADD'L COMPONENTS
Orthopedic
248d
Cleared
May 09, 1990
MODULAR HIP SYSTEM
Orthopedic
90d
Cleared
Feb 15, 1990
UNI-POLAR HEAD
Orthopedic
90d
Cleared
Jan 04, 1990
INTRAMEDULLARY HIP SCREW
Orthopedic
136d
Cleared
Nov 21, 1989
TRICON-M TOTAL KNEE SYSTEM
Orthopedic
368d
Cleared
Nov 20, 1989
ZIRCONIA CERAMIC HEAD ADD'L SIZES
Orthopedic
25d
Cleared
Nov 17, 1989
PAPPAS TRI-FLANGE VENTILATION TUBE
Ear, Nose, Throat
88d
Cleared
Nov 16, 1989
RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS
Orthopedic
199d
Cleared
Sep 01, 1989
ZIRCONIA CERAMIC HEAD (YITRIA STABILIZED)
Orthopedic
267d
Cleared
Jul 19, 1989
POROUS GENESIS PATELLAR AND STEMLESS TIBIAL COMP.
Orthopedic
188d
Cleared
Jul 19, 1989
POROUS GENESIS STEMMED TIBIAL COMPONENT
Orthopedic
104d
Cleared
Apr 19, 1989
POROUS COATED GENESIS FEMORAL COMPONENT
Orthopedic
135d
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