9 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
COMFIT FPOWDER FREE EXAMINATION GLOVERS (HYPOALLERGENIC)
FDA 510(k)
FDA Class 1
·General Hospital
TECHDEVICE OCCLUSION BALLOON CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
X-VIEW, IMAGEN
FDA 510(k)
FDA Class 2
·Radiology
RETROFLEX 3 DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code NPT·February 8, 2013
UNIPLEX NANOLINE CANNULA
FDA Adverse Event
Other
·PAJUNK GMBH MEDIZINTECHNOLOGIE·Product code BSP·December 22, 2010
EXPRESS? LD VASCULAR
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code FGE·July 22, 2014
EVOLUT FX VALVE
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·March 10, 2026
EVOLUT FX VALVE
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·March 10, 2026
Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-23, c) 44, 47, 50, 53 head, Large, Item Number 314-13-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-25; Shoulder Arthroplasty
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·April 10, 2024