Depuy Ireland Uc

FDA Filings

This page includes the latest FDA filings for Depuy Ireland Uc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3015516266
FEI Number3015516266
NameDepuy Ireland UC
Owner & OperatorDePuy Synthes, Inc.
Contact Address700 Orthopaedic Drive
Warsaw IN 46582 US
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressLoughbeg, Ringaskiddy
Co. Cork Munster, Munster IE
Establishment Type
  • Manufacture Medical Device
  • Develop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
DePuy Ireland UC
DePuy PINNACLE Dual Mobility Liner2020-09-11
DePuy Ireland UC
SIGMA High Performance (HP) Partial Knee System2020-04-16
Depuy Ireland UC [DePuy Synthes, Inc.]
DELTA XTEND Reverse Shoulder System2020-02-28
Depuy Ireland UC [DePuy Synthes, Inc.]
DELTA XTEND Reverse Shoulder System2020-02-28
Depuy Ireland UC [DePuy Synthes, Inc.]
ATTUNE All Polyethylene Tibia2020-02-18
DePuy Ireland UC
ATTUNE All-Polyethylene Tibia2020-01-30
Depuy Ireland UC [DePuy Synthes, Inc.]
DELTA XTEND Reverse Shoulder System2019-12-06
Depuy Ireland UC [DePuy Synthes, Inc.]
DELTA XTEND Reverse Shoulder System2019-12-06
DePuy Ireland UC
GLOBAL UNITE Platform Shoulder System2018-01-11
Depuy Ireland UC [DePuy Synthes, Inc.]
Attune2017-06-29
Depuy Ireland UC [DePuy Synthes, Inc.]
Attune2017-06-29

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