34 results · 27ms · Sources: EU EUDAMED, US FDA

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PRIMACONNEX RD AND WD ESTHETIC CONTOUR ZI ABUTMENTS

FDA 510(k)
FDA Class 2 ·Dental

MEDTRONIC PS MEDICAL CHANNELSCOPE ENDOSCOPE, MODELS 2232-001, 2232-002, 2232-003, 2232-004, 2233-002, 2233-005

FDA 510(k)
FDA Class 2 ·Neurology

SOFT TISSUE SCREW AND WASHER

FDA 510(k)
FDA Class 2 ·Orthopedic

LINEAR 3-6

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 19, 2020

CAPSUREFIX NOVUS

FDA Adverse Event
Death ·MPRI·Product code DTB·April 23, 2013

EQUIPMENT DELIVERY SYSTEM , OSC-600

FDA Adverse Event
Malfunction ·STRYKER COMMUNICATIONS·Product code BRY·April 21, 2011

CAPSURE SP NOVUS

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 10, 2008

MAXPLUS POSITIVE PRESSURE CONNECTOR

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·July 30, 2021

MAXPLUS POSITIVE PRESSURE CONNECTOR

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·July 7, 2021

BD MAXPLUS¿ NEEDLELESS CONNECTOR

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 16, 2021

MAXPLUS CLEAR NEEDLE-FREE CONNECTOR

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FPA·January 16, 2020

BD MAXPLUS¿ NEEDLELESS CONNECTOR

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·October 26, 2022

MAXPLUS CLEAR NEEDLE-FREE CONNECTOR

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FPA·January 16, 2020

MAXPLUS POSITIVE PRESSURE CONNECTOR

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·June 10, 2021

MAXPLUS POSITIVE PRESSURE CONNECTOR

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 14, 2020

BD MAXPLUS¿ NEEDLELESS POSITIVE PRESSURE CONNECTOR

FDA Adverse Event
Malfunction ·Product code FPA·September 27, 2021

MAXPLUS POSITIVE PRESSURE CONNECTOR

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·July 30, 2021

CAPIOX FX OXYGENATOR

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·May 22, 2025

CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·December 5, 2022

CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·December 16, 2022