24 results · 23ms · Sources: EU EUDAMED, US FDA

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NeuGuide

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

MERIT EMBOLECTOMY CATHETER MODEL ASAP100

FDA 510(k)
FDA Class 2 ·Cardiovascular

BALANCED KNEE SYSTEM MODULAR REVISION KNEE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

CAPSUREFIX NOVUS

FDA Adverse Event
Malfunction ·MPRI·Product code DTB·June 10, 2013

SILVERHAWIK LS-M

FDA Adverse Event
EV-3 INC·Product code MCW·July 8, 2011

HS LONG 5MM CURVED SHEARS

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code GEI·September 11, 2008

vyaire Flexible Patient Circuit, 3100A, REF 29028-004, intended to be used with the 3100A High Frequency Oscillatory Ventilator (HFOV)

FDA Enforcement
Class II ·Completed·Vyaire Medical·December 13, 2023

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·May 7, 2018

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017