7 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPE
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
Ventura NanoMetalene System
FDA UDI
Seaspine Orthopedics Corporation·10889981152215·Ventura NM Trial, 11mm x 32mm x 09mm, Lordotic
A.I.M. KNOTLESS MENISCAL REPAIR DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ISOAID ADVANTAGE PD-103, MODEL IAPD-103A
FDA 510(k)
FDA Class 2
·Radiology
ENCOR BREAST BIOPSY PROBE
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·April 3, 2014
OBTRYX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·January 29, 2013
PLUM A+ 11.6 POLAND
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code FRN·December 20, 2010