33 results · 36ms · Sources: EU EUDAMED, US FDA

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Single-Use Surgical Mask With Ear Loop

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

HHM

FDA UDI
Oticon A/S·05707131357434·G300 SC, MINIRITE R LI-ION 2.4G C047 HHM

Dornier MedTech

FDA UDI
Dornier MedTech GmbH·04049958000225·Medilas D MultiBeam Diode Laser, D-Plug

NA

FDA UDI
Synthes GmbH·10886982142573·2.4MM CORTEX SCREW 3.5MM HEAD/SELF-TAPPING 42MM

CODMAN

FDA UDI
Cerenovus, Inc.·10886704066804·CODMAN SLIM-LINE Aneurysm Clip 45 Degree Angle ...

ABSORBENT PAPER POINTS

FDA UDI
DiaDent Group International·08806383554596·"An absorbent paper points is an endodontic pap...

ABSORBENT PAPER POINTS

FDA UDI
DiaDent Group International·08806383512800·"An absorbent paper points is an endodontic pap...

LIFELINES PHOTIC STIMULATOR

FDA 510(k)
FDA Class 2 ·Neurology

V-Print splint

FDA 510(k)
FDA Unclassified ·Unknown

STENT - VASCULAR RECONSTRUCTION

FDA Adverse Event
Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·May 11, 2018

STENT - VASCULAR RECONSTRUCTION

FDA Adverse Event
Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·May 11, 2018

STENT - VASCULAR RECONSTRUCTION

FDA Adverse Event
Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·May 11, 2018

STENT - VASCULAR RECONSTRUCTION

FDA Adverse Event
Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·May 11, 2018

STENT - VASCULAR RECONSTRUCTION

FDA Adverse Event
Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·May 14, 2018

JETSTREAM® XC ATHERECTOMY CATHETER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MCW·December 6, 2016

JETSTREAM® XC ATHERECTOMY CATHETER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MCW·December 6, 2016

SPRINT QUATTRO SECURE

FDA Adverse Event
Injury ·MPRI·Product code LWS·April 7, 2016

SPRINT QUATTRO SECURE S

FDA Adverse Event
Malfunction ·MPRI·Product code LWS·June 9, 2016

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 27, 2014

HS III PROXIMAL SEAL SYSTEM 3.8MM

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·August 4, 2011