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