24 results · 22ms · Sources: EU EUDAMED, US FDA

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Sphynx™

FDA 510(k)
FDA Class 2 ·Orthopedic

DIGITAL EYE-FUNDUS CAMERA

FDA 510(k)
FDA Class 2 ·Ophthalmic

LERADO, POWER WHEELCHAIR

FDA 510(k)
FDA Class 2 ·Physical Medicine

KYPHON HV-R BONE CEMENT

FDA Adverse Event
Injury ·MDT KYPHON NEUCHATEL MFG·Product code NDN·October 25, 2017

KYPHX® HV-R¿ BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·April 7, 2017

KYPHX HV-R BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·July 19, 2020

CONTOUR NEXT

FDA Adverse Event
Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code NBW·November 22, 2021

KYPHX® HV-R¿ BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 4, 2019

KYPHX® HV-R¿ BONE CEMENT

FDA Adverse Event
Injury ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 17, 2017

KYPHX HV-R BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·December 17, 2018

CONTOUR NEXT

FDA Adverse Event
Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code NBW·July 16, 2021

KYPHX® HV-R¿ BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 7, 2017

CONTOUR NEXT (CONNECTED)

FDA Adverse Event
Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code NBW·April 29, 2021

KYPHX HV-R BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·October 12, 2017

KYPHX HV-R BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·July 9, 2020

CONTOUR NEXT

FDA Adverse Event
Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code NBW·December 1, 2023

ANALYZER CABLE

FDA Adverse Event
Malfunction ·MEDTRONIC INC.·Product code KRG·October 10, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

ALLEGRETTO WAVE

FDA Adverse Event
Malfunction ·WAVELIGHT GMBH·Product code LZS·June 16, 2011

BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·June 22, 2022