32 results · 23ms · Sources: EU EUDAMED, US FDA

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PRESSON ELECTRODE

FDA 510(k)
FDA Class 2 ·Neurology

MODIFICATION TO M2376A DEVICELINK SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

MAGNETOM AERA; MAGNETOM SKYRA

FDA 510(k)
FDA Class 2 ·Radiology

FLANGE FIXTURE AND ABUTMENT

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·June 20, 2016

BIA400 IMPLANT 4MM W ABUTMENT 8MM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·April 28, 2016

BIA400 IMPLANT 4MM W ABUTMENT 12MM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·October 11, 2016

FLANGE FIXTURE AND ABUTMENT

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·June 26, 2016

BIA400 IMPLANT 4MM W ABUTMENT 8MM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·May 25, 2016

BIA400 IMPLANT 4MM WITH ABUTMENT 12MM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·June 6, 2016

FLANGE FIXTURE AND ABUTMENT

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·July 21, 2016

BIA400 IMPLANT 4MM W ABUTMENT 12MM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·January 13, 2016

ENTUIT GASTROSTOMY BR BALLOON RETENTION FEEDING TUBE WITH ENFIT CONNECTION

FDA Adverse Event
Injury ·XERIDIEM MEDICAL DEVICES·Product code PIF·April 18, 2018

BIA400 IMPLANT 4MM W ABUTMENT 10MM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·October 5, 2015

ASKU

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·December 12, 2025

COCHLEAR BAHA ATTRACT SYSTEM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 14, 2016

BIA400 IMPLANT 4MM W ABUTMENT 8MM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·March 18, 2016

VICTORY XL DR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 13, 2014

OT PING ENHANCED METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013

FLAIR ENDOVASCULAR STENT GRAFT

FDA Adverse Event
Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code MIH·June 6, 2011

FLANGE FIXTURE AND ABUTMENT

FDA Adverse Event
Injury ·COCHLEAR LTD·Product code MAH·September 1, 2016