45 results
·
34ms
·
Sources: EU EUDAMED, US FDA
OLYMPUS GUIDE WIRE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SeaSpine Spacer System - Pacifica™
FDA UDI
Seaspine Orthopedics Corporation·10889981058777·Pacifica Trial, 9mm x 20mm x 17mm
SeaSpine Spacer System - Pacifica™
FDA UDI
Seaspine Orthopedics Corporation·10889910058779·Pacifica Trial, 9mm x 20mm x 17mm
C-GRAFT
FDA 510(k)
FDA Class 2
·Dental
EXPRESS LD BILIARY PREMOUNTED STENT SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
EXPRESS LD ILIAC / BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code NIO·January 8, 2026
EXPRESS LD ILIAC / BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code NIO·August 14, 2025
EXPRESS LD ILIAC / BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code NIO·December 4, 2025
EXPRESS LD ILIAC / BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code NIO·December 4, 2025
EXPRESS LD ILIAC / BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code NIO·November 5, 2025
EXPRESS LD ILIAC / BILIARY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NIO·March 25, 2026
EXPRESS LD ILIAC / BILIARY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NIO·November 21, 2024
EXPRESS LD ILIAC / BILIARY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NIO·March 6, 2025
EXPRESS LD ILIAC / BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code NIO·October 29, 2025
EXPRESS LD ILIAC / BILIARY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NIO·August 6, 2025
EXPRESS LD ILIAC / BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code NIO·May 1, 2026
EXPRESS LD ILIAC / BILIARY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NIO·November 21, 2024
VIRTUOSO
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·June 10, 2014
TRANSVENE RV
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code LWS·April 10, 2018
DEPUY ASR XL FEM IMP SIZE 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·January 29, 2013