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

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Hamilton-C6

FDA 510(k)
FDA Class 2 ·Anesthesiology

HAMILTON-C6

FDA Adverse Event
Malfunction ·HAMILTON MEDICAL AG·Product code CBK·February 10, 2025

Dornier MedTech

FDA UDI
DORNIER MEDTECH AMERICA, INC.·00810116023158·DMTL SmartFlex 270 High Energy Reusable (5X)

Dornier MedTech

FDA UDI
DORNIER MEDTECH AMERICA, INC.·00810116023172·DMTL SmartFlex 600 High Energy Reusable (5X)

Dornier MedTech

FDA UDI
DORNIER MEDTECH AMERICA, INC.·00810116023189·DMTL SmartFlex 1000 High Energy Reusable (5X)

CODMAN

FDA UDI
Cerenovus, Inc.·10886704001515·CODMAN SLIM-LINE Aneurysm Clip Bayonet Blade Le...

Life Instruments

FDA UDI
Life Instrument Corporation·M93072016580SFC0·S-Lift Cobb, 16mm

Life Instruments

FDA UDI
Life Instrument Corporation·M93072016580C0·Custom Cobb 16"7" handle 1/2

Accuvue+

FDA 510(k)
FDA Class 2 ·Radiology

WATERLASE MD TURBO PLUS MODEL 7200XXX

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

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

RESOLUTE INTEGRITY RX

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code NIQ·July 14, 2017

ONYX

FDA Adverse Event
Injury ·MEDTRONIC COVIDIEN·Product code MFE·July 5, 2016

PROTEGE EVERFLEX SELF-EXPANDING STENT SYSTEM STANDARD

FDA Adverse Event
Death ·COVIDIEN·Product code FGE·July 14, 2017

PROTEGE EVERFLEX SELF-EXPANDING STENT SYSTEM STANDARD

FDA Adverse Event
Injury ·COVIDIEN·Product code FGE·July 14, 2017

SPRINT QUATTRO SECURE

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2011

ISOLINE

FDA Adverse Event
Injury ·SORIN GROUP ITALIA SRL·Product code MRM·June 28, 2013

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014

ONYX

FDA Adverse Event
Injury ·MEDTRONIC COVIDIEN·Product code MFE·July 5, 2016

ONYX

FDA Adverse Event
Injury ·MEDTRONIC COVIDIEN·Product code MFE·July 5, 2016