23 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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