97 results · 25ms · Sources: EU EUDAMED, 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