15 results · 26ms · Sources: EU EUDAMED, US FDA

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MAGEC 2 Spinal Bracing and Distraction System

FDA 510(k)
FDA Class 2 ·Orthopedic

Oticon

FDA UDI
Oticon A/S·05707131283856·RIA2, MINIBTE 312 WL 85 STG

SSW CARBIDE TRIMMING AND FINISHING

FDA UDI
Ss White Burs, Inc.·D6901508852·12 BLADE FINISHING CARBIDE 7006 - 5 PACK

FETAL MONITOR MODEL: BT-200T

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

OLYMPUS ULTRASONIC SURGICAL SYSTEM SONOSURG

FDA 510(k)
FDA Unclassified ·Unknown

LINEAR ST

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 16, 2024

BD MULTI-CHECK CD4 LOW CONTROL

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·August 29, 2023

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 6, 2013

PRSVN FB TIB TRAY LM/RL CEM S3

FDA Adverse Event
Injury ·DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS·Product code HRY·June 29, 2011

AUTOVENT 4000 WITH CPAP

FDA Adverse Event
Malfunction ·ALLIED HEALTHCARE PRODUCTS, INC.·Product code BTL·August 27, 2008

DIVA

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

DIVA

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

SENRI

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code DQY·December 25, 2016

BD MULTI-CHECK CD4 LOW CONTROL

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·August 16, 2023

METACROSS RX PTA BALLOON DILATATION CATHETER

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·October 15, 2019