25 results · 36ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

DC-70/DC-70T /DC-70 Pro/DC-70 Exp/DC-75/DC-78/DC-70S Diagnostic Ultrasound System

FDA 510(k)
FDA Class 2 ·Radiology

M2A MODULAR HIP SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304209268·

COLIN PRESS MATE, MODEL BP S510

FDA 510(k)
FDA Class 2 ·Cardiovascular

GE LOGIQ I, LOGIQ E AND VIVID E

FDA 510(k)
FDA Class 2 ·Radiology

MOTO PARTIAL KNEE ANATOMICAL FEMORAL COMPONENT CEMENTED S6 RM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·January 17, 2022

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·June 25, 2025

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 11, 2013

GYNECARE X-TRACT MORCELLATOR

FDA Adverse Event
Malfunction ·ETHICON·Product code HET·July 15, 2011

CONTOUR TEST STRIPS (50)

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE LLC.·Product code NBW·September 9, 2008

Merit Inflation Syringe Kit. Catalog Number KOS-02857

FDA Recall
Terminated ·Merit Medical Systems, Inc.·Product code MAV·August 25, 2016

UNKNOWN SHELL

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWY·August 14, 2017

M2A TPR HI CARBON 41/32MM LNR

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWY·February 23, 2018

FLEXCATH ADVANCE STEERABLE SHEATH

FDA Adverse Event
Injury ·MEDTRONIC CRYOCATH LP·Product code DRA·July 17, 2017

ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

FDA Adverse Event
Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·July 17, 2017

ACHIEVE MAPPING CATHETER

FDA Adverse Event
Injury ·MEDTRONIC MEXICO·Product code DRF·July 17, 2017

MOTO PARTIAL KNEE TIBIAL TRAY FIX CEMENTED S7 RM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·October 10, 2018

MODULAR TAPERLOC FEMORAL

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWY·August 14, 2017

UNKNOWN LINER

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWY·August 14, 2017

M2A-T M/H RAD 2HL SHL 41/54MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 23, 2018

M2A TAPER LINER

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWY·August 17, 2017