29 results
·
21ms
·
Sources: EU EUDAMED, US FDA
FEMTO LDV(TM) Z-GENERATION FEMTOSECOND SURGICAL LASER
FDA 510(k)
FDA Class 2
·Ophthalmic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813872·GENUMEDI PRO SILVER SIZE VII
Trivicta
FDA UDI
Ortho Development Corporation·00822409123858·Collar EXT Size 7
TALOS®-C HA
FDA UDI
MEDITECH SPINE, LLC·B167521312070·
SAFETY RELEASE ARCH BAR KIT
FDA 510(k)
FDA Class 2
·Dental
NEODENT IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
VACUTRON
FDA UDI
Allied Medical, LLC·00026072005385·CONTINUOUS SUCTION REGULATORS
COOK® CERVICAL RIPENING BALLOON
FDA Adverse Event
Malfunction
·COOK INC·Product code PFJ·July 18, 2016
VACUTRON
FDA UDI
Allied Medical, LLC·00026072005422·CONTINUOUS SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072005439·CONTINUOUS SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072005415·CONTINUOUS SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072005408·CONTINUOUS SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072005392·CONTINUOUS SUCTION REGULATORS
COOK® CERVICAL RIPENING BALLOON
FDA Adverse Event
Malfunction
·COOK INC·Product code PFJ·July 19, 2016
GREENLIGHT MOXY FIBER OPTIC
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS·Product code GEX·May 23, 2013
STERRAD
FDA Adverse Event
Malfunction
·ADVANCED STERILIZATION PRODUCTS·Product code FRC·September 22, 2014
ATTAIN STARFIX
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 16, 2011
ADVANCE 35 LP LOW PROFILE BALLOON CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code DQY·February 3, 2017
ADVANCE 35 LP LOW PROFILE BALLOON CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code DQY·March 10, 2017
CARTO 3
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·September 16, 2024