29 results · 21ms · Sources: EU EUDAMED, US FDA

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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