97 results
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25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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speX Support Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
38 MM MODULAR HEAD PROVISIONAL
FDA UDI
Biomet Orthopedics, LLC·00880304003125·
PLAYTEX GENTILE GLIDE, PLAYTEX GENTILE GLIDE MULTIPACK TAMPONS
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
CONTINUUM AND TRILOGY INTEGRATED TAPER (IT) ACETABULAR SYSTEMS; LONGEVITY IT HIGHLY CROSSLINKED POLYETHYLENE ELEVATED LI
FDA 510(k)
FDA Class 2
·Orthopedic
M2A 38MM MOD HD STD NK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·May 5, 2014
UNKNOWN M2A HIP
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·September 27, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 15, 2014
ONYX, AVM
FDA Adverse Event
Injury
·EV3 NEUROVASCULAR·Product code MFE·June 17, 2013
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·July 23, 2011
M2A 38MM MOD HD +3MM NK
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·November 3, 2017
M2A 38MMX54MM CUP
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·May 25, 2023
BI-METRIC/X POR NC LAT 14X150
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·January 23, 2018
M2A-38 CUP NON FLARED SZ 56MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·May 23, 2018
COLLARLESS BI-METRIC POROUS STEM ALLIANCE X-SERIES
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·April 7, 2017
M2A 1 PC SHELL 38MMX56MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·December 27, 2017
BI-METRIC/X POR NC LAT 16X160
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·December 28, 2017
M2A 38MM MOD HD -6MM NK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·August 29, 2014
M2A-38 CUP 50MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·April 5, 2017
M2A ACETABULAR CUP
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·August 15, 2017
M2A-38 CUP NON FLARED SIZE 58MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·April 27, 2018