Stanmore Implants Worldwide , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stanmore Implants Worldwide , Ltd. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Stanmore Implants Worldwide , Ltd. has 8 FDA 510(k) cleared medical devices. Based in Washington, Dc, US.
Historical record: 8 cleared submissions from 2011 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Stanmore Implants Worldwide , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stanmore Implants Worldwide , Ltd.
8 devices
Cleared
Jan 20, 2015
PATIENT SPECIFIC DISTAL FEMORAL
Orthopedic
287d
Cleared
Jan 22, 2014
JTS EXTENDIBLE DISTAL FEMORAL IMPLANT
Orthopedic
61d
Cleared
Jan 11, 2013
SCULPTOR ROBOTIC GUIDANCE ARM (RGA)
Orthopedic
210d
Cleared
Sep 20, 2012
METS MODULAR PROXIMAL FEMUR
Orthopedic
167d
Cleared
Sep 19, 2012
METS MODULAR DISTAL FEMUR
Orthopedic
167d
Cleared
Sep 19, 2012
METS MODULAR TOTAL FEMUR
Orthopedic
166d
Cleared
Sep 05, 2012
METS SMILES TOTAL KNEE REPLACEMENT
Orthopedic
156d
Cleared
Mar 22, 2011
JTS EXTENDEABLE IMPLANT
Orthopedic
615d