9 results
·
28ms
·
Sources: EU EUDAMED, US FDA
CLARUS SERIES 2100 ENDOSCOPE
FDA 510(k)
FDA Class 2
·Orthopedic
Solstice Occipito-Cervico-Thoracic System
FDA UDI
Life Spine, Inc.·00190837016807·
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 27, 2024
CLEARPATH ALIGNER
FDA 510(k)
FDA Class 2
·Dental
TRELLIS-6 PERIPHERAL INFUSION SYSTEM (140CM CATHETER LENGTH 10CM INFUSION LENGTH)
FDA 510(k)
FDA Class 2
·Cardiovascular
STARDRIVE SCRWDRVR SHFT/T4 50MM/SELF-RETAINING/HXC
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXX·November 16, 2020
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·January 22, 2013
ATTAIN OTW
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010
OPTISENSE
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014