31 results · 27ms · Sources: EU EUDAMED, US FDA

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ANKYLOS DENTAL IMPLANT SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

SOAR Retractor System

FDA UDI
SPINEOLOGY INC.·M7403041509·15mm x 90mm Portal Tube

STOCKERT V172 SERIES VENOUS FEMORAL CANNULAE

FDA 510(k)
FDA Class 2 ·Cardiovascular

BARRETT UNICONDYLAR TIBIAL BEARING

FDA 510(k)
FDA Class 2 ·Orthopedic

DYNASTY(R) COCR LINER

FDA Adverse Event
Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·September 10, 2018

UNKNOWN

FDA Adverse Event
Malfunction ·COOK, INC.·Product code DTK·August 21, 2014

UNK

FDA Adverse Event
Injury ·COOK, INC.·Product code DTK·August 20, 2014

UNKNOWN

FDA Adverse Event
Injury ·COOK INC·Product code DTK·August 20, 2014

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·April 8, 2013

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 24, 2011

CONTAK RENEWAL 3

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS, INC·Product code NIK·May 8, 2008

GUNTHER TULIP VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·April 3, 2026

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·December 5, 2017

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Malfunction ·COOK INC·Product code DTK·November 1, 2017

GUNTHER TULIP VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·November 4, 2025

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·February 27, 2018

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·May 5, 2017

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Malfunction ·COOK INC·Product code DTK·May 12, 2017

UNKNOWN

FDA Adverse Event
Injury ·Product code DTK·August 20, 2020

UNK

FDA Adverse Event
Injury ·COOK, INC.·Product code DTK·August 20, 2014