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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Malfunction ·COCHLEAR LTD.·Product code MCM·August 23, 2016

NUCLEUS 22

FDA Adverse Event
Injury ·COCHLEAR LIMITED·Product code MCM·May 18, 2025

ETS FLEX ARTICNG LNR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·March 5, 2013

DEPUY ORTHOPAEDICS PINNACLE SECTOR II CUPS, SZ 56, 40MM DIAM, 56 OUTER

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·February 14, 2011

CARELINK

FDA Adverse Event
Malfunction ·MEDTRONIC MILACA, INC.·Product code NVZ·August 7, 2014

IMMULITE® 2000 PSA

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code MTF·April 26, 2023

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 17, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Death ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 17, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015

SIMILAR DEVICE NS7TBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·November 10, 2014

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·March 5, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·March 4, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·February 6, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·March 4, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·March 6, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·February 13, 2015