59 results · 22ms · Sources: EU EUDAMED, US FDA

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Vector Hammertoe Correction System

FDA 510(k)
FDA Class 2 ·Orthopedic

NuVasive

FDA UDI
Nuvasive, Inc.·00195377046413·NTS Standard Tube, 18x50mm

Ion Coagulation Pen

FDA UDI
ION MEDICAL, INC.·B9122018502·18 Gauge Bipolar Coagulation Pen

CODMAN

FDA UDI
Cerenovus, Inc.·10886704002383·CODMAN AVM Micro Clip Applier No 1

Blade Handle

FDA UDI
KATENA PRODUCTS, INC.·00841668112380·BARD-PARKER HANDLE #3

SYNTHES (USA) 1.3 MM CRANIOFACIAL SCREWS

FDA 510(k)
FDA Class 2 ·Dental

SPACELABS BLEASESIRIUS ANESTHESIA WORKSTATION

FDA 510(k)
FDA Class 2 ·Anesthesiology

AORTIC TAG THORACIC ENDOPROSTHESIS (CTAG)

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code MIH·April 2, 2019

AORTIC TAG THORACIC ENDOPROSTHESIS (CTAG)

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code MIH·April 2, 2019

UNKNOWN SYMBOTEX MESH

FDA Adverse Event
Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·May 2, 2019

UNKNOWN PARIETEX

FDA Adverse Event
Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·May 2, 2019

VALIANT STENT GRAFT

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code MIH·July 17, 2018

VALIANT STENT GRAFT

FDA Adverse Event
Death ·MEDTRONIC IRELAND·Product code MIH·July 17, 2018

CONSULTA CRT-D

FDA Adverse Event
Injury ·MEDTRONIC MED REL, INC.·Product code NIK·August 11, 2011

ASCENSIA CONTOUR

FDA Adverse Event
Injury ·BAYER HEALTHCARE, LLC·Product code NBW·October 15, 2008

IMMULITE 2000 PROSTATE SPECIFIC ANTIGEN

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code MTF·July 2, 2013

VALIANT STENT GRAFT

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MIH·July 17, 2018

GMK SPHERE CEMENTLESS

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MBH·May 25, 2026

GMK SPHERE TOTAL KNEE SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·November 21, 2024

GMK SPHERE TOTAL KNEE SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·May 5, 2025