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

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EBI PERIARTICULAR PLATING SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

JOBST forMen

FDA UDI
BSN MEDICAL, INC.·04042809871081·FOR MEN 15-20 MM HG THIGH MICRO DOT BAND OPEN T...

P3IMRT TM

FDA 510(k)
FDA Class 2 ·Radiology

MERTEX-PLUS REUSABLE SURGICAL DRAPE

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

36MM COCR BIOMET FEM HD STD NK

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWA·June 13, 2016

UNKNOWN EXCEED HIP

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWA·August 5, 2016

UNKNOWN RECAP 48MM HEAD

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWA·September 16, 2016

36MM 12/14 TPR FEM HEAD -4 NK

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWA·June 28, 2016

EXCEED ABT M2A-36 MOD HEAD

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWA·June 28, 2016

EXCEED ABT RINGLOC-X SHELL

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWA·July 20, 2017

M2A MOD HD COCR DIA28/+3MM T1

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWA·December 23, 2015

32MM COCR BIOMET FEM HD STD NK

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWA·February 16, 2016

RECAP/MAGNUM ACETABULAR SHELL

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWA·February 15, 2017

EXCEED ABT M2A-36 MOD HEAD -3MM T1

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWA·June 1, 2016

TENSION FREE VAGINAL TAPE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code OTN·April 9, 2013

WRISTORE DISTAL RADIUS FRACTURE FIXATOR

FDA Adverse Event
Malfunction ·ZIMMER, INC.·Product code KTT·February 15, 2011

VENTAK PRIZM 2 VR

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008

RECAP SHELL COCR PC DIA56/50MM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWA·September 1, 2016

36MM COCR BIOMET FEM HD +6 NK

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWA·September 7, 2018

EXCEED ABT STD SHELL PC DIA50M M

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWA·July 16, 2016