50 results · 24ms · Sources: EU EUDAMED, US FDA

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reVive Light Therapy LED Cleansing System

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

YANKAUER SUCTION TUBE

FDA UDI
SONTEC INSTRUMENTS, INC.·B0991804470·YANKAUER SUCTION TUBE CHROME

YANKAUER SUCTION TUBE

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896000575·YANKAUER SUCTION TUBE CHROME

Fixed Ankle Clamp

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215063764·

MYOSCIENCE CRYO-TOUCH

FDA 510(k)
FDA Class 2 ·Neurology

SURGICRAFT SCREW FIXATION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·May 5, 2020

INSPIRE 8F M

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA·Product code DTZ·January 3, 2024

GYNECARE TVT EXACT CONTINENCE SYSTEM

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTN·June 20, 2013

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·July 27, 2011

BECTON DICKINSON 10 ML SYRINGE LUER-LOK TIP

FDA Adverse Event
Other ·BECTON DICKINSON·Product code FMF·September 29, 2008

INSPIRE 8F M

FDA Adverse Event
Injury ·SORIN GROUP ITALIA·Product code DTZ·January 4, 2024

INSPIRE OXYGENATOR

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA·Product code DTZ·March 12, 2026

INSPIRE OXYGENATOR

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA·Product code DTZ·March 12, 2026

INSPIRE 8F

FDA Adverse Event
Injury ·SORIN GROUP ITALIA·Product code DTZ·November 5, 2025

INSPIRE 8F

FDA Adverse Event
Injury ·SORIN GROUP ITALIA·Product code DTZ·November 5, 2025

INSPIRE OXYGENATOR

FDA Adverse Event
Injury ·SORIN GROUP ITALIA·Product code DTZ·December 11, 2025

INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·April 20, 2021

INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·September 11, 2020

BD VIPER¿ LT SYSTEM

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code OOI·August 14, 2023