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

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585

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

COMPACT TOUCH STS

FDA 510(k)
FDA Class 2 ·Radiology

X-VOID, SPIDER

FDA 510(k)
FDA Class 2 ·Orthopedic

ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code NKB·October 18, 2017

ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·February 13, 2020

CRESCENT SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MSD DEGGENDORF MFG·Product code MAX·April 11, 2022

U BY KOTEX UNKNOWN : TAMPON, MENSTRUAL, UNSCENTED : HEB

FDA Adverse Event
Malfunction ·BERRY PLASTICS QINGDAO LTD.·Product code HEB·October 31, 2022

U BY KOTEX : TAMPON, MENSTRUAL, UNSCENTED : HEB

FDA Adverse Event
Malfunction ·BERRY PLASTICS QINGDAO LTD.·Product code HEB·January 5, 2022

INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT,

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code MAX·November 16, 2018

U BY KOTEX UNKNOWN : TAMPON, MENSTRUAL, UNSCENTED : HEB

FDA Adverse Event
Malfunction ·BERRY PLASTICS QINGDAO LTD.·Product code HEB·June 28, 2023

CRESCENT SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MSD DEGGENDORF MFG·Product code MAX·November 13, 2018

CAPSTONE PTC SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·July 8, 2020

CRESCENT SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MSD DEGGENDORF MFG·Product code MAX·December 7, 2017

CRESCENT SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MSD DEGGENDORF MFG·Product code MAX·April 1, 2020

CRESCENT SYSTEM

FDA Adverse Event
Malfunction ·MSD DEGGENDORF MFG·Product code MAX·October 11, 2021

CRESCENT SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MSD DEGGENDORF MFG·Product code MAX·March 22, 2019

CRESCENT SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MSD DEGGENDORF MFG·Product code MAX·January 7, 2019

9600

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 5, 2013

LVAS KIT, HM-II, EUROPEAN, EP

FDA Adverse Event
Malfunction ·THORATEC CORP.·Product code DSQ·June 15, 2011

APEX PUSH MONORAIL

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC·Product code LOX·September 18, 2008