24 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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