8 results
·
17ms
·
Sources: EU EUDAMED, US FDA
DSL ACTIVE BETA2-MICROGLOBULIN (DSL 6500)
FDA 510(k)
FDA Class 2
·Immunology
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0155080·Trial, Drill Guide, 15 x 12, 8mm, Tapered
NERVE LOCATOR/MONITOR SYSTEM, MODIFICATION
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
MAGNA SURGEONS GOWNS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SETROX S 45
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code NVZ·January 9, 2013
ACCURUS 400VS
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CTR·Product code HQC·February 26, 2014
ARTERIAL CATH SET: 20 GA X 8
FDA Adverse Event
Malfunction
·ARROW INTL., INC.·Product code DQX·November 5, 2010
Pipeline Flex Embolization Device
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021