49 results · 21ms · Sources: EU EUDAMED, US FDA

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XACT Robotic System

FDA 510(k)
FDA Class 2 ·Radiology

EarQ

FDA UDI
Oticon A/S·05707131353702·G40 S, MINIRITE T 312 2.4G C091 EARQ

16PW - Krispy Kreme FAK - Poly White

FDA UDI
Certified Safety Manufacturing, Inc.·00766588015064·16PW - Krispy Kreme FAK - Poly White

XTRA AUTOTRANSFUSION SYSTEM

FDA 510(k)
FDA Class 2 ·Anesthesiology

SECURE RELINE/PICKUP MATERIAL

FDA 510(k)
FDA Class 2 ·Dental

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

XIVE

FDA Adverse Event
Injury ·DENTSPLY TULSA·Product code DZE·October 17, 2008

GREENLIGHT ADDSTAT

FDA Adverse Event
Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·August 4, 2011

PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2013

ACCUTRAK DELIVERY CATHETER SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·November 28, 2017

FAST-CATH¿ TRANSSEPTAL GUIDING INTRODUCER SWARTZ¿ SL TRANSSEPTAL SERIES 63 CM LE

FDA Adverse Event
Injury ·ST. JUDE MEDICAL·Product code DYB·September 4, 2019

UNKNOWN MOM HIP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 12, 2017

UNKNOWN MOM HIP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 11, 2017

COREVALVE TRANSCATHETER AORTIC VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·October 18, 2017

UNKNOWN BIOMET TIBIAL COMPONENT

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·August 4, 2017

UNKNOWN HIP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 3, 2017

COREVALVE TRANSCATHETER AORTIC VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·October 17, 2017

UNKNOWN HIP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 3, 2017

UNKNOWN HIP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 3, 2017

UNKNOWN ZIMMER TIBIAL COMPONENT

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JWH·August 4, 2017