45 results · 34ms · Sources: EU EUDAMED, US FDA

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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