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

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M2424A SONOS 5500/4500 DIAGNOSTIC ULTRASOUND SYSTEM, VERSION B.2. 21330A TRANSDUCER

FDA 510(k)
FDA Class 2 ·Radiology

Mariner MIS

FDA UDI
Seaspine Orthopedics Corporation·10889981171490·MIS Tap A/O, Dia 4.75mm

Metal Custom Rx

FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746104183·BRACKET INTER TWIN V-SLOT MAND BICUSPID 022 TQ=...

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361009108·PedFuse Reset, CNL, 8.0mm x 70mm

E-Z LINK CROSS CONNECTOR

FDA 510(k)
FDA Class 2 ·Orthopedic

BIOLOK SCREW

FDA 510(k)
FDA Class 2 ·Orthopedic

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 17, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·October 7, 2020

LIGASURE

FDA Adverse Event
Injury ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·July 21, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 20, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 26, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 9, 2021

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 2, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 13, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 16, 2019

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·April 24, 2020

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·March 14, 2019

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 16, 2021

PROMUS ELEMENT ¿

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·March 13, 2013

LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 10.0CM

FDA Adverse Event
Malfunction ·ALLERGAN·Product code LTI·January 28, 2011