9 results
·
16ms
·
Sources: EU EUDAMED, US FDA
MICROBACT 12A SYSTEM, 12B SYSTEM, AND 24E SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
ABN ANEROID SPHYGMOMANOMETER
FDA 510(k)
FDA Class 2
·Cardiovascular
ANATOMIC PEEK CERVICAL FUSION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CERTAIN¿ TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code NHA·July 27, 2023
MALLINKCKRODT
FDA Adverse Event
Malfunction
·COVIDIEN·Product code BTS·May 13, 2014
ALLURA XPER FD10
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code IZI·November 4, 2010
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·January 12, 2013
CERTAIN¿ TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code NHA·July 27, 2023
Pipeline Flex Embolization Device
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021