7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
THERATRON 1000
FDA 510(k)
FDA Class 2
·Radiology
MBK SURGEONS'(STERILE & NON-STERILE) SURG GLOVES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
TRELLIS 6 120X30
FDA Adverse Event
Malfunction
·COVIDIEN·Product code KRA·November 4, 2010
SERVO-I
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code CBK·February 6, 2014
ZELTIQ COOLCORE (6.3)
FDA Adverse Event
Injury
·ZELTIQ AESTHETICS INC.·Product code OOK·December 27, 2012
Pipeline Flex Embolization Device
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021