2,009 results · 37ms · Sources: EU EUDAMED, US FDA

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Breathe+

FDA 510(k)
FDA Class 2 ·Anesthesiology

OsteoMed

FDA UDI
OSTEOMED LLC·00845694020848·FPS 2.0mm x 18mm Locking Screw

Altus Spine Interbody Fusion System

FDA UDI
Altus Spine, LLC·00843210131672·Broach Trial

75H - Class B 21 - Swing Out Door

FDA UDI
Certified Safety Manufacturing, Inc.·00766588620183·75H - Class B 21 - Swing Out Door

Sapphire NC ULTRA Coronary Dilatation Catheter

FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955982156·

OsteoMed

FDA UDI
OSTEOMED LLC·00845694075183·FPS 2.0 x 18mm Locking Screw Sterile Qty 5

OP300

FDA 510(k)
FDA Class 2 ·Radiology

RHIGENE ANA ELISA TEST SYSTEM, MODEL K7560

FDA 510(k)
FDA Class 2 ·Immunology

PRECISION

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 6, 2008

STRYKEFLOW II

FDA Adverse Event
Injury ·STRYKER ENDOSCOPY·Product code GCX·August 18, 2011

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION CORPORATION·Product code FRN·July 3, 2013

NUCLEUS FREEDOM IMPLANT WITH CONTOUR ADVANCE ELECTRODE

FDA Adverse Event
Injury ·COCHLEAR LTD·Product code MCM·August 21, 2018

NUCLEUS CI512 COCHLEAR IMPLANT WITH CONTOUR ADVANCE ELECTRODE

FDA Adverse Event
Malfunction ·COCHLEAR LTD·Product code MCM·March 21, 2018

DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code PQF·June 21, 2018

BIA400 IMPLANT 4MM W ABUTMENT 8MM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·March 21, 2018

NUCLEUSCI512 COCHLEAR IMPLANT WITH CONTOUR ADVANCE ELECTRODE

FDA Adverse Event
Injury ·COCHLEAR LTD·Product code MCM·February 22, 2018

TRUERESULT

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·July 16, 2015

TRUERESULT

FDA Adverse Event
Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·September 15, 2021

BLOOD GLUCOSE SYSTEM

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·October 2, 2015

AMS 800 URINARY CONTROL SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EZY·September 11, 2019