28 results · 24ms · 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-80/DC-80 PRO/DC-80 EXP/DC-80S/DC-85 Diagnostic

FDA 510(k)
FDA Class 2 ·Radiology

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776412982·7Fr 34cm Semi Rigid Biopsy Cup Forceps Serrated...

CARDINAL HEALTH

FDA UDI
Cardinal Health 200, LLC·10887488481074·ORTHO PACK

MYSPINE MC VERTEBRA L04

FDA Adverse Event
Malfunction ·MEDACTA INTERNATIONAL SA·Product code PQC·July 6, 2018

UBM PLUS

FDA 510(k)
FDA Class 2 ·Radiology

VANTAGECATH INTRAVASCULAR CATHETER

FDA 510(k)
FDA Class 2 ·General Hospital

REDUCTION CANNULATED PEDICLE SCREW 5X45

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·February 17, 2023

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

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

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·April 8, 2016

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·April 8, 2016

MYSPINE S01 DRILL BASED GUIDE

FDA Adverse Event
Malfunction ·MEDACTA INTERNATIONAL SA·Product code PQC·December 12, 2018

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·July 31, 2017

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 29, 2017

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 29, 2017

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 12, 2019

MYSPINE-MC DRILL GUIDE L03

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code PQC·May 26, 2023

MYSPINE STOPPER SLEEVE 30 MM, DRILL2.7 - LUMBAR

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LXH·February 26, 2020

MAXCORE DISPOSABLE BIOPSY SYSTEM

FDA Adverse Event
Malfunction ·BARD REYNOSA SA DE CV·Product code KNW·October 10, 2014

TOTALCARE BARIATRIC PLUS BED

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·June 11, 2013

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 23, 2011