24 results · 23ms · Sources: EU EUDAMED, US FDA

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UNIVERSAL GLENOID - CENTRAL SCREW 20MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·February 26, 2024

FREESTYLE LITE

FDA Adverse Event
Malfunction ·Product code NBW·April 6, 2010

ECLIPSE CAGE SCREW S, 30MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·December 16, 2019

ARTHREX ECLIPSE HUMERAL HEAD, 41/16

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·December 16, 2019

ECLIPSE TRUNION,41 MM TPS CTD

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·December 16, 2019

ARTHREX ECLIPSE HUMERAL HEAD, 41/16

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·January 23, 2023

ECLIPSE CAGE SCREW M, 35MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·January 23, 2023

UNIVERS VAULTLOCK GLENOID, SMALL

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code KWS·January 23, 2023

ARTHREX ECLIPSE HUMERAL HEAD, 41/16

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·December 4, 2019

ECLIPSE TRUNION,41 MM TPS CTD

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·December 4, 2019

ECLIPSE CAGE SCREW S, 30MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·December 4, 2019

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 3, 2013

SPECTRUM INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 1, 2014

SOLYX SIS SYSTEM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·December 21, 2010

GLENOID, PE WITH PEG, SMALL

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code KWS·December 4, 2019

GLENOID, PE WITH PEG, SMALL

FDA Adverse Event
Malfunction ·Product code KWS·April 5, 2021

ECLIPSE CAGE SCREW M, 35MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·April 9, 2021

ECLIPSE TRUNION,41 MM TPS CTD

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·April 9, 2021

ECLIPSE CAGE SCREW M, 35MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code QHQ·February 26, 2024

UNIVERS REVERS GLENOID

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code PHX·February 26, 2024