10,000 results · 221ms · Sources: EU EUDAMED, US FDA

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VIDEOARTHROSCOPE, HD, 4MM X 30 DEG

FDA Adverse Event
Malfunction ·SMITH & NEPHEW, INC.·Product code HRX·October 16, 2017

GENESIS II

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS·Product code JWH·December 5, 2011

INTERTAN

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC·Product code HWC·June 2, 2011

HEMI HEAD 56MM

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code KWY·April 10, 2019

BHR ACETABULAR CUP 60MM

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·September 11, 2019

ACC COCR CBL 2.0 W/CLMP SAMPLE

FDA Adverse Event
Malfunction ·SMITH & NEPHEW, INC.·Product code JWH·December 4, 2019

TRUCATH

FDA Adverse Event
Injury ·BROOKS MANUFACTURING SITE·Product code BSP·June 14, 2010

EXOGEN COUPLING GEL

FDA Adverse Event
Injury ·BROOKS MANUFACTURING SITE·Product code MUI·June 20, 2010

ECHELON

FDA Adverse Event
Injury ·SMITH AND NEPHEW, INC.·Product code LPH·June 2, 2011

HEMI HEAD 46MM

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·July 10, 2019

SMITH AND NEPHEW INC.

FDA Adverse Event
Injury ·SMITH AND NEPHEW INC·Product code NBH·March 19, 2007

SMITH & NEPHEW, INC

FDA Adverse Event
Injury ·SMITH & NEPHEW INC·Product code GAD·May 29, 2001

BHR ACETABULAR CUP 56MM

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·March 5, 2019

EXOGEN

FDA Adverse Event
Injury ·BROOKS MANUFACTURING SITE·Product code LOF·June 20, 2010

HEMI HEAD 50MM

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code JDH·November 27, 2018

TRAUMA IMPLANT

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JDS·December 31, 2019

ACETABULAR CUP HAP SIZE 52/58

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·December 28, 2019

EXOGEN COUPLING GEL

FDA Adverse Event
Injury ·BROOKS MANUFACTURING SITE·Product code MUI·June 23, 2010

EXOGEN

FDA Adverse Event
Injury ·BROOKS MANUFACTURING SITE·Product code LOF·June 20, 2010

EXOGEN COUPLING GEL

FDA Adverse Event
Injury ·BROOKS MANUFACTURING SITE·Product code MUI·June 20, 2010