29 results · 23ms · 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.

ACON OXY II ONE STEP OXYCODONE TEST STRIP; TEST DEVICE

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

EISENHUT INSTRUMENTE GMBH

FDA registration
EISENHUT INSTRUMENTE GMBH·32 products·🇩🇪 Germany

ZEUS-P

FDA UDI
SPINAL ELEMENTS, INC.·00840606160841·FLAT PADDLE DISTRACTOR, 7MM

MEDRELIEF

FDA 510(k)
FDA Class 2 ·Neurology

COSMO TENS PF-990 MINI DIGITAL WIRELESS PATCH

FDA 510(k)
FDA Class 2 ·Neurology

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

IBP ELB INT. ULNA LRG RGT LNG STM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDC·June 24, 2016

ASR XL TAP SLV ADAP 12/14+2

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·April 9, 2013

STENOSCOP

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·March 28, 2011

ENDOTAK RELIANCE

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·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