26 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ZELTIQ CoolSculpting System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MINI CPAP DEVICE AND HUMIDIFIER ACCESSORY
FDA 510(k)
FDA Class 2
·Anesthesiology
OSTEOSYMBIONICS, ST TEMPORALIS IMPLANT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·June 18, 2019
BELLAFILL DERMAL FILLER
FDA Adverse Event
Injury
·SUNEVA MEDICAL, INC.·Product code LMH·July 30, 2019
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·October 14, 2014
7.3MM CANNULATED LOCKING SCEW
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·July 8, 2011
PULSE GEN MODEL 102
FDA Adverse Event
Injury
·CYBERONICS INC·Product code LYJ·June 14, 2013
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
INVISION¿ TOTAL ANKLE SYSTEM
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY INC·Product code HSN·July 18, 2022