68 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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