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

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INVISION Total Ankle Revision System

FDA 510(k)
FDA Class 2 ·Orthopedic

INVISION¿ TOTAL ANKLE SYSTEM

FDA Adverse Event
Injury ·WRIGHT MEDICAL TECHNOLOGY INC·Product code HSN·July 18, 2022

BACTRACK LCD ALCOHOL DETECTOR

FDA 510(k)
FDA Class 1 ·Clinical Toxicology

SURESIGNS VM4, SURESIGNS VM6, SURESIGNS VM8 MODEL: 863063, 863064, 863065, 863066, 863068

FDA 510(k)
FDA Class 2 ·Cardiovascular

BIZACT

FDA Adverse Event
Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·June 18, 2019

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·February 6, 2019

NON AC-POWERED PATIENT LIFT

FDA Adverse Event
Malfunction ·INVACARE REHABILITATION EQUIP·Product code FSA·October 14, 2014

STARCLOSE VASCULAR CLOSURE SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·June 14, 2013

SAGITTAL BLADE

FDA Adverse Event
Malfunction ·STRYKER IRELAND LTD.·Product code GFA·June 29, 2011

BIZACT

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·April 30, 2024

BIZACT

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·April 30, 2024

BIZACT

FDA Adverse Event
Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020

BIZACT

FDA Adverse Event
Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020

BIZACT

FDA Adverse Event
Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020

BIZACT

FDA Adverse Event
Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·October 21, 2020

BIZACT

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·April 30, 2024

BIZACT

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·May 2, 2024

BIZACT

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·May 24, 2024

BIZACT

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·April 25, 2024

BIZACT

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·May 17, 2024