54 results · 41ms · 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.

Arthrosurface WristMotion Total Wrist Arthroplasty System

FDA 510(k)
FDA Class 2 ·Orthopedic

SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

CHROMOSTREAK

FDA 510(k)
FDA Class 1 ·Microbiology

UNK MAMMARY IMPLANT

FDA Adverse Event
Injury ·ALLERGAN (COSTA RICA)·Product code FWM·July 10, 2025

PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code NEW·April 22, 2018

PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code NEW·April 22, 2018

PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code NEW·April 22, 2018

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·April 22, 2018

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·April 22, 2018

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·April 22, 2018

BD VACUTAINER® MULTIPLE SAMPLE LUER ADAPTER

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·March 21, 2019

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

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

EASY CORE BIOPSY DEVICE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FCG·November 5, 2009

EASY CORE BIOPSY DEVICE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FCG·November 5, 2009

EASY CORE BIOPSY DEVICE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FCG·November 5, 2009

EASY CORE BIOPSY DEVICE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FCG·November 5, 2009

EASY CORE BIOPSY DEVICE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FCG·November 5, 2009

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code DTK·October 7, 2012

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code DTK·October 7, 2012

RX ACCULINK CAROTID STENT SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code NIM·October 8, 2007