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

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Analyzer, Medical Image

FDA Pre-Market Approval
FDA Class 2 ·LOGICON CARIES DETECTOR

Analyzer, Medical Image

FDA Pre-Market Approval
FDA Class 2 ·LOGICON CARIES DETECTOR

Analyzer, Medical Image

FDA Pre-Market Approval
FDA Class 2 ·LOGICON CARIES DETECTOR

Analyzer, Medical Image

FDA Pre-Market Approval
FDA Class 2 ·Logicon Caries Detection Software

Analyzer, Medical Image

FDA Pre-Market Approval
FDA Class 2 ·LOGICON CARIES DETECTOR

DeltaForm HD

FDA UDI
Merz Dental GmbH·D7091980025·DeltaForm HD lower posteriors, M, A3 -MADE IN G...

DeRoyal

FDA UDI
DEROYAL INDUSTRIES, INC.·00749756047937·Bias Stockinette 2In X 5Yd1/Pk 20/Cs

PEREGRINE TAPERED DIFFUSION PROBE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Malfunction ·COCHLEAR LTD.·Product code MCM·August 23, 2016

ANSPACH***REF 98-0025***Custom MDA Tube for use with MA-D20 Attachment***Rx Only*** This device is intended to be used with Anspach Systems

FDA Enforcement
Class II ·Terminated·The Anspach Effort, Inc.·July 2, 2014

INTERSTIM II

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·February 17, 2019

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 5, 2014

INTEGRATED APD SET W/CASSETTE3-PRONG

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·February 7, 2011

CLOSUREFAST CATHETER

FDA Adverse Event
Malfunction ·COVIDIEN·Product code GEI·September 27, 2016

INTERSTIM II

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·January 24, 2019

PULSE GENERATOR, PERMANENT, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code NVZ·June 9, 2016

ADAPTA DR

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015

ADAPTA D

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 17, 2015

SIMILAR DEVICE NS7TCBL174HS, PMA # P990025

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015