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

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DILATOR TUBE SET

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

MODEL 733HC GRAVITY/VACUUM STEAM STERILIZER

FDA 510(k)
FDA Class 2 ·General Hospital

EDGE CO2 LASER SYSTEM

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

GMK HINGE FEMUR SIZE 2 RIGHT

FDA Adverse Event
Injury ·Product code KRO·September 12, 2014

GMK HINGE FEMUR SIZE 5 RIGHT

FDA Adverse Event
Injury ·MEDACTA INTERNAIONAL SA·Product code KRO·August 21, 2014

GMK REVISION TOTAL KNEE SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 15, 2025

GMK HINGE AND REVISION TINBN COATED

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 7, 2025

GMK-HINGE FIXED TIBIAL TRAY SIZE 4 R

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·October 29, 2020

GMK-REVISION FEMUR REVISION PS SIZE 2 R

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·November 11, 2020

GMK-REVISION FEMUR REVISION PS #4 R

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 23, 2021

GMK-REVISION FIXED TIBIAL TRAY CEMENTED SIZE 1 RIGHT

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 14, 2016

GMK-REVISION FEMUR REVISION PS SIZE 4 RIGHT

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 8, 2016

GMK-REVISION FEMUR REVISION PS SIZE 2 R

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·February 7, 2020

GMK-REVISION TIBIAL AUGMENTATION SIZE 4/5MM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·October 3, 2019

GMK-REVISION FIXED TIBIAL INSERT SC SIZE 4/17MM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 19, 2019

GMK-REVISION, FEMUR REVISION PS #5 R

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·January 8, 2016

GMK-HINGE FIXED TIBIAL INSERT SIZE 2/14MM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·June 28, 2017

3.0MM TI STERNAL LOCKING SCREW SELF-DRILLING/16MM

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HWC·May 20, 2013

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·September 26, 2014

PCA II

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 10, 2011