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

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BIOCHECK HUMAN CARDIAC TROPONIN-I IMMUNOASSAY TEST KIT

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

SureFlex

FDA UDI
AMERICAN MEDICAL SYSTEMS·00878953000183·550 µm Lithotripsy Fiber

Diamond D

FDA UDI
Keystone Industries·H66810130621·Denture Acrylic HC Light 1 lb P& L

Dornier MedTech

FDA UDI
DORNIER MEDTECH AMERICA, INC.·04049958003097·270 micron Holmium Laser Fiber Cable, Single Us...

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033454244·

Cosmolock

FDA UDI
Kalitec Direct LLC·B07311K0130120·Segmental Rod Reducer Driver

STYROFOAM CUTTERS FOR BLOCK CASTING SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

BACTEC MGIT 960 SIR KITS

FDA 510(k)
FDA Class 2 ·Microbiology

50-13062 DEKALB VASCULAR PACK

FDA Adverse Event
Malfunction ·DEROYAL INDUSTRIES, INC.·Product code KDD·June 17, 2002

SCHILLER

FDA Adverse Event
Malfunction ·SCHILLER AG·Product code MHX·November 2, 2006

UNKNOWN KUDO ELBOW

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

DISC LT DSTL HMRL BDY SET

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDC·April 1, 2019

UNKNOWN KUDO ELBOW

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

UNKNOWN KUDO ELBOW

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

UNKNOWN KUDO ELBOW

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

UNKNOWN KUDO ELBOW

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

UNKNOWN KUDO ELBOW

FDA Adverse Event
Death ·BIOMET UK LTD.·Product code JDC·May 19, 2017

UNKNOWN KUDO ELBOW

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 1, 2013

CAPSUREEPI

FDA Adverse Event
Injury ·MPRI·Product code DTB·August 15, 2014