8 results
·
25ms
·
Sources: EU EUDAMED, US FDA
MENTOR UNISTENT URETERAL STENT SET
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Arthrex®
FDA UDI
ARTHREX, INC.·00888867523951·Spine Compression Screw, 5.0x38mm
BREAST & FOREIGN BODY LOCALIZATION INSTRUMENT
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SURGISTEEL
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code NIQ·June 16, 2014
FLEXTEND II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·October 19, 2010
HEARTMATE II LEFT VENTRICULAR ASSIST DEVICE
FDA Adverse Event
Death
·THORATEC CORP.·Product code DSQ·December 12, 2012
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·October 18, 2022