Depuy(Ireland) is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Depuy(Ireland) - FDA 510(k) Cleared Devices
Recent clearances: GLOBAL ICON Stemless Shoulder System, DELTA XTEND(TM) Reverse Shoulder System, DePuy Corail AMT Hip Prosthesis
13
Total
13
Cleared
0
Denied
Depuy(Ireland) has 13 FDA 510(k) cleared orthopedic devices. Based in Cork, IE.
Last cleared in 2022. Active since 2010.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by DePuy Orthopaedics, Inc., Depuy Orthopaedies, Inc. and Depuy Orthopajedics, Inc.. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Depuy(Ireland)
13 devices
Cleared
CT
Jan 19, 2022
GLOBAL ICON Stemless Shoulder System
Orthopedic
148d
Cleared
Feb 24, 2020
DELTA XTEND(TM) Reverse Shoulder System
Orthopedic
143d
Cleared
Nov 01, 2019
DePuy Corail AMT Hip Prosthesis
Orthopedic
260d
Cleared
Oct 08, 2019
Attune Revision LPS Inserts
Orthopedic
98d
Cleared
Oct 04, 2019
Delta Xtend Revers Shoulder System
Orthopedic
28d
Cleared
May 17, 2019
Delta Xtend Reverse Shoulder System
Orthopedic
193d
Cleared
Jun 15, 2017
ATTUNE Cemented Tibial Base, Fixed Bearing
Orthopedic
90d
Cleared
Jul 19, 2016
DePuy Actis DuoFix Hip Prosthesis
Orthopedic
109d
Cleared
Jun 10, 2016
ATTUNE Revision Knee System
Orthopedic
88d
Cleared
Feb 13, 2015
DEPUY ATTUNE KNEE SYSTEM - CEMENTLESS CR AND PS FEMORAL COMPONENETS
Orthopedic
312d
Cleared
Apr 03, 2014
DEPUY GLOBAL UNITE SHOULDER SYSTEM
Orthopedic
107d
Cleared
Dec 15, 2010
DEPUY GLOBAL UNITE SHOULDER SYSTEM
Orthopedic
153d
Cleared
Nov 23, 2010
DEPUY RECLAIM REVISION HIP SYSTEM
Orthopedic
120d