8 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
PROGRESS GUIDE WIRE FAMILY, PILOT GUIDE WIRE FAMILY
FDA 510(k)
FDA Class 2
·Cardiovascular
IMTEC SENDAX MDI ORTHO6 AND ORTHO8
FDA 510(k)
FDA Class 2
·Dental
EXSALT SD7 WOUND DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
GMK-PRIMARY TIBIAL INSERT UC FIXED SIZE 3 / 14 MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·October 30, 2018
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·February 6, 2019
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 21, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 26, 2014
CAPSUREFIX
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011