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

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TRIDENT CROSSFIRE POLYUETHYLENE LINERS

FDA 510(k)
FDA Class 2 ·Orthopedic

Natus

FDA UDI
XLTEK·00382830047258·Natus Brain Monitor

OneTouch Ultramini

FDA UDI
LifeScan Europe GmbH·00353885002677·OneTouch Ultramini Blood Glucose Monitoring Sys...

Specials

FDA UDI
Seaspine Orthopedics Corporation·10889981162436·QC Trial, 7x24, 11mm

IM-9A MICROINJECTORS

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

SUCTION PUMP FOR INTRACORPOREAL ULTRASOUND LITHOTRIPTER AND ACCESSORIES, MODEL 2207.XXX

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

NATUS BRAIN MONITOR BREAKOUT

FDA Adverse Event
Malfunction ·NATUS MEDICAL INCORPORATED·Product code OLV·July 13, 2023

CRYSTALENS ACCOMODATING IOL

FDA Adverse Event
Injury ·BAUSCH + LOMB·Product code NAA·April 1, 2013

NXSTAGE SYSTEM ONE

FDA Adverse Event
Death ·NXSTAGE MEDICAL, INC.·Product code KDI·September 23, 2021

DEXTRUS 4136

FDA Adverse Event
Injury ·BIOTRONIK SE & CO. KG·Product code NVN·March 26, 2013

8800

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·February 25, 2011

LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·March 28, 2008

Natus Brain Monitor Breakout Box, Part Number 021911; full-montage standard electroencephalograph

FDA Recall
Open, Classified ·Natus Neurology DBA Excel Tech., Ltd. (XLTEK)·Product code GWQ·June 18, 2025

UNKNOWN EMPRINT ANTENNA

FDA Adverse Event
Injury ·COVIDIEN LP - SUPERDIMENSION INC·Product code NEY·June 24, 2022

Natus Brain Monitor Breakout Box, Part Number 021911; full-montage standard electroencephalograph

FDA Enforcement
Class II ·Ongoing·Natus Neurology DBA Excel Tech., Ltd. (XLTEK)·July 30, 2025

670G INSULIN PUMP MMT-1780KL

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·December 16, 2021

WATCHMAN LAA CLOSURE DEVICE & DELIVERY SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·February 5, 2021

NATUS BRAIN MONITOR BREAKOUT

FDA Adverse Event
Malfunction ·NATUS MEDICAL INCORPORATED DBA EXCEL-TECH LTD.·Product code OMB·June 25, 2025

NATUS BRAIN MONITOR BREAKOUT

FDA Adverse Event
Malfunction ·NATUS MEDICAL INCORPORATED DBA EXCEL-TECH LTD.·Product code OMB·June 25, 2025

PLATE, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HRS·September 22, 2016