26 results · 23ms · Sources: EU EUDAMED, US FDA

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CLEARCUT S SAFETY KNIFE

FDA 510(k)
FDA Class 1 ·Ophthalmic

Leva® Anterior Interbody System

FDA UDI
Spine Wave, Inc.·10840642108804·Modular Spacer, SSA, 26 mm (W) x 26 mm (L) x 15...

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450160145·

4D-VIEW 9.1 (4D VIEW PC SOFTWARE) MODEL: H48651SZ

FDA 510(k)
FDA Class 2 ·Radiology

IMAGYN ISOSLEEVE / ISOSTAR NEEDLE SYSTEM

FDA 510(k)
FDA Class 1 ·Radiology

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·October 6, 2023

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·November 9, 2023

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·May 7, 2025

QUICK CHECK ONE

FDA Adverse Event
DIAGNOSTIC SOLUTIONS, INC.·Product code CFR·April 10, 1997

QUICK CHECK ONE

FDA Adverse Event
DIAGNOSTIC SOLUTIONS, INC.·Product code CFR·March 17, 1997

ATTUNE FB TIB BASE SZ 4 CEM

FDA Adverse Event
Injury ·DEPUY IRELAND - 9616671·Product code JWH·October 16, 2019

MAXCEM ELITE

FDA Adverse Event
Malfunction ·KERR CORPORATION·Product code EMA·May 13, 2013

QC F/K-WIRES Ø0.6-3.2 F/532.001 532.010

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HWE·September 23, 2014

M2A MODULAR HEAD COMPONENT 38MM HEAD DIAMETER

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 1, 2011

PEDIASAT

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES PR·Product code DRE·December 10, 2025

EDWARDS OXIMETRY CENTRAL VENOUS CATHETER

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES·Product code DXG·January 7, 2025

EDWARDS OXIMETRY CENTRAL VENOUS CATHETER

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES PR·Product code DQE·March 27, 2025

EDWARDS OXIMETRY CENTRAL VENOUS CATHETER

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES·Product code DXG·January 7, 2025

QUICK CHECK ONE

FDA Adverse Event
DIAGNOSTIC SOLUTIONS, INC.·Product code CFR·April 17, 1997

DEKA SMARTXIDE² TRIO

FDA Adverse Event
Malfunction ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·October 31, 2023