16 results · 18ms · Sources: EU EUDAMED, US FDA

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DISPOPROPHY

FDA 510(k)
FDA Class 2 ·Dental

artegral life

FDA UDI
Merz Dental GmbH·D7091993182·anteriors; shade B1; mould ITM

SET GRI-FILL 3.0

FDA 510(k)
FDA Class 2 ·General Hospital

Evis Exera III Duodenovideoscope Olympus TJF-Q190V

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JDI·June 18, 2024

EVIS EXERA III DUODENOVIDEOSCOPE

FDA Adverse Event
Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·February 18, 2022

FOXCROSS PTA BALLOON

FDA Adverse Event
Injury ·ABBOTT VASCULAR·Product code LIT·February 27, 2013

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 7, 2011

CONSULTA CRT-D

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014

INFUSE(R) Bone Graft, SMALL KIT, REF 7510200, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic

FDA Recall
Terminated ·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013

INFUSE(R) Bone Graft, LARGE KIT, REF 7510600, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic

FDA Recall
Terminated ·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013

INFUSE(R) Bone Graft, MEDIUM KIT, REF 7510400, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic

FDA Recall
Terminated ·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013

INFUSE(R) Bone Graft, SMALL KIT, REF 7510200AUS, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic

FDA Recall
Terminated ·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013

INFUSE(R) Bone Graft, MEDIUM KIT, REF 7510400AUS, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic

FDA Recall
Terminated ·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013

INFUSE(R) Bone Graft, LARGE II KIT, REF 7510800AUS, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic

FDA Recall
Terminated ·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013

INFUSE(R) Bone Graft,LARGE II KIT, REF 7510800, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic

FDA Recall
Terminated ·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013