686 results · 24ms · Sources: EU EUDAMED, US FDA

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PFF-1

FDA 510(k)
FDA Class 2 ·Anesthesiology

FILTER, INFUSION BLOOD (1 PFF-100)

FDA 510(k)
FDA Class 2 ·General Hospital

UNKNOWN HIP FEMORAL STEM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWY·August 22, 2022

UNK HIP FEMORAL STEM CHARNLEY

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code LPH·July 26, 2022

UNK HIP FEMORAL STEM C-STEM

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code LPH·July 26, 2022

UNK HIP FEMORAL STEM SUMMIT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 25, 2022

ARTICULEZE M HEAD 36MM +8.5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code LZO·November 15, 2016

UNKNOWN STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LZO·July 13, 2025

UNK STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LZO·July 15, 2025

PINNACLE MTL INS NEUT40IDX56OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·May 25, 2018

ASPHERE M SPEC 12/14 40 +8.5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code KWA·May 25, 2018

SROM*STM ST,30+4L NK,18X13X160

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·June 20, 2018

PINN MAR +4 10D 28IDX50OD

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code LPH·June 20, 2018

S-ROM M HEAD 36MM +3

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·June 20, 2018

S-ROM*HEAD FEMORAL COCR 28+6

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code JDI·June 20, 2018

PINNACLE MTL INS NEUT36IDX52OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·June 20, 2018

UNK HIP FEMORAL STEM C-STEM

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code LPH·July 26, 2022

UNK HIP FEMORAL STEM CORAIL

FDA Adverse Event
Injury ·DEPUY IRELAND - 9616671·Product code LZO·July 26, 2022

UNKNOWN HIP FEMORAL CONSTRUCT ACTIS

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LZO·January 20, 2026

UNKNOWN HIP FEMORAL CONSTRUCT SUMMIT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LZO·January 20, 2026