23 results · 24ms · Sources: EU EUDAMED, US FDA

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EMG CTA01-XXX SERIES PURO OXYGEN CONCENTRATOR

FDA 510(k)
FDA Class 2 ·Anesthesiology

NA

FDA UDI
Stryker GmbH·00886385005683·Cortical Screw, Self-tap., T10 Drive

SureLOK Mini Posterior Cervical/Upper Thoracic System

FDA UDI
PRECISION SPINE, INC.·00840019907118·3.5mm x 20mm SureLOK™ PC Screw

Symmetry Metzenbaum

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482051566·Symmetry® Scissors, Metzenbaum Dissecting, Curv...

NIDO Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07315K0430200·Sagittal Bender, Double Ended Left

NEXAN SYSTEM, MODEL NX-300

FDA 510(k)
FDA Class 2 ·Cardiovascular

BLUEPHASE

FDA 510(k)
FDA Class 2 ·Dental

HNM Medical

FDA UDI
HNM STAINLESS, LLC.·00842962107669·METZENBAUM SCISSORS, 8", SLIM DELICATE, CVD

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·November 15, 2013

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code KWP·November 15, 2013

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014

SECURE 3 MED/SURG BEDOBS 01/13

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·April 9, 2013

ISYMM ASPHERIC INTRAOCULAR LENS

FDA Adverse Event
Malfunction ·HOYA SURGICAL OPTICS, INC.·Product code HQL·February 25, 2011

VITALITY DS

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014

VERSA-DIAL 42X18X46 HUM HEAD

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code HSD·November 19, 2021